Work schedule standard (mon-fri) environmental conditions office job description are you an ambitious and proven professional looking for an exceptional opportunity to showcase your strong work ethic and skills? thermo fisher scientific inc. is seeki...
Location/division specific information our multidisciplinary modelling and simulation experts design and implement health economic models that describe complex medical processes to understand and evaluate the implications of clinical trials; demonstrate the value of interventions beyond efficacy, and assess benefits, risks, and the economic consequences associated with healthcare interventions. this role offers 100% remote working flexibility. discover impactful work: if you have a passion for health economic modeling to conduct cost-effectiveness analyses of healthcare interventions and have experience conceptualizing and implementing simulation models (, discrete event simulation) and other decision-analytic models (, decision trees, markov, individual state-transition, survival partition), a position in modelling and simulation at evidera is waiting for you! a day in the life: implement simulation models (, discrete event simulation) and other decision-analytic models (, decision trees, markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. support scientific and financial project management, scoping, tracking progress, and teamwork for multiple projects. implement one or more of the following under direction: design and development of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions. program models using microsoft excel with visual basic for applications (vba) or simulation specialised software. conduct literature reviews with emphasis on extracting...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. discover impactful work: provides administrative safety support to the safety reporting team and pharmacovigilance department. responsible for tasks related to receipt and submission of expedited and periodic safety reports, including quality check tasks, pertaining to the department’s projects. assists management in producing project metrics as required. involved in projects and programs relating to safety reporting and may take a lead role on projects. alerts manager to any quality or timeline issues and takes a proactive approach in the identification and resolution of such issues. may also be involved in updates to procedures and other initiatives related to safety reporting. may mentor or train new central safety reporting staff. hybrid working type a day in the life: • recei...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. our project delivery colleagues within our ppd® clinical research services direct, coordinate and lead the technical and operational aspects of projects, securing the successful completion of clinical trials. this includes collaborating with functional area leads to identify and evaluate fundamental issues on the project and to ensure that solutions are implemented. project delivery is vital to helping our customers deliver life-changing therapies. through our global team, you may engage in diverse initiatives and projects, or be part of a virtual international project team gaining cross-cultural experience. therapeutic scope include **general medicine **(dermatology, gi, (uc/cd) liver, nephrology, cardiovascular, metabolic (obesity & diabetes).** **discover impactful work**: we ...
**work schedule** standard (mon-fri) **environmental conditions** office **are you an ambitious professional seeking to excel in a dynamic sales environment? thermo fisher scientific inc., a world-class leader in serving science, is looking for a dedicated account manager iii to join our team in colombia. this is an outstanding opportunity to contribute to a company that makes a global impact on health, safety, and the environment.**: **responsibilities**: - successfully implement and manage key and strategic accounts within the colombian market. - develop and implement ambitious strategies to drive growth and maintain a top clinical market share. - collaborate with internal teams to deliver flawless service and support to clinical and research customers. - cultivate and uphold positive relationships with key clients to understand their needs and offer tailored solutions. - strictly adhere to company policies and ethical standards while competing in the marketplace. **requirements**: - proven experience in sales, specifically within the laboratory equipment, consumables, or biotechnology sectors. - comprehensive understanding of the colombian market and its outstanding dynamics. - outstanding communication and negotiation skills to effectively manage customer relationships. - ability to build, develop, and implement strategies that align with company objectives. - demonstrated ability to work both independently and as part of a collaborative team to achieve goals....
Our team of colleagues in clinical research services are at the forefront of getting cures to market. we bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. our clinical research team, who powers our ppd® clinical research portfolio, are part of our leading global contract research organization (cro). we are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.are you a data and a people person? here’s your team. we manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. we work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust.as a clinical data team lead, you will help ensure the highest quality of data and effectiveness of clinical trail data. you will work directly with senior clinical data team leads to create, monitor and close studies in a timely manner. this position also works with sites, clients, and other team members at ppd.at ppd we hire the best, develop ourselves and each other, and recognize the p...
The** technical application specialist iii** is a member of our global customer services team. the role provides high quality first - and second-line support to customers in the context of products supplied by digital science business unit. the high quality demanded by this position will be met by the analyst’s ability to respond to support incidents within target times and assist in activities designed to facilitate continuous improvements to help-desk services. **what will you do?** - communicate with customers in a professional and courteous manner - create and manage incidents through the incident lifecycle according to current guidelines and procedures - adhere to escalation procedures and customer service level agreements - provide technical solutions to incidents wherever possible - participate in a weekend roster for supporting customers needing 24 x 7 support. - work to resolve incidents with other digital science departments including development, techops, and services to provide resolution to customer issues related to hosted and on-premise systems. - backup team leader in matters of dealing with customer complaints and issues - offer direction and skill training to other technical analysts on the team - proactively learn and participate in training on new technologies as well as supported products - be self-motivated and make best use of available time - provide expertise in the installation of customer product updates - maintain processes, tools, and documentation in support of the customer environments. - participate in in practical process imp...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. **discover impactful work**: the principal business information analyst leads discussions with the business to identify key performance metrics to provide insights into performance and is accountable for the timely and accurate production of reports and is allocated as metrics lead to initiatives to implement improvements. in this role you will provide guidance and support for complex ad hoc queries and demonstrate a solid understanding of the industry and associated benchmarks, using this knowledge to provide valuable insight into performance. **a day in the life**: - performs exploratory data analysis to surface data and identify trends. performs review on completed deliverables before sending to customer. - takes ownership for achieving deliverables within the specified time ...
Work schedule standard (mon-fri) environmental conditions office job description here’s what you’ll do: - works with global regulatory lead(s), regulatory strategists, global regulatory sub-teams and project teams regarding the development and execution of regulatory strategy through the product development lifecycle. - coordinate, develop and contribute to content and format of regulatory submissions and related supplements and amendments, including fda meeting requests, briefing books, inds, ctas, pediatric plans, dsurs, maa/bla/nda, etc. - identify and assess regulatory risks for assigned projects or programs. - senior manager may serve as point of contact with regulatory agencies relevant to assigned projects or programs, as appropriate. - ability to work both independently and within project teams, committees, etc. to achieve group goals. - accountable for tracking, following up and archiving correspondence, regulatory commitments, and queries from health agencies here’s what you’ll bring to the table: - ba/bs degree in a scientific/engineering/healthcare discipline required, masters, pharmd or phd preferred. - 5+ years of experience in the pharmaceutical industry preferred in latam countries. - 3+ years of experience in regulatory strategy or relevant training/experience preferred - experience in infectious diseases and/or biologicals is preferred - strong knowledge of current us and eu regulations - strong experience with ctd format and content of regulatory filings - exceptional written and oral communication in english and spanish. - knowl...
Ppd’s (a part of thermo fisher scientific) mission is to improve health. it starts as an idea to find a cure. it becomes a life saved. all in-between, it’s you! we know that meaningful results not only require the right approach, but also the right people. we invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. our project delivery team directs, coordinates and leads the technical and operational aspects of projects, securing the successful completion of clinical trials. the team is therapeutically aligned to respond better to our customer needs. the therapeutic scope includes general medicine, hematology and oncology (hemonc), infectious and respiratory diseases (ird), cardiovascular, metabolic and critical care (cvmet), neuroscience, vaccines and fsp/client-dedicated. as a clinical team manager (ctm), you combine deep knowledge, therapeutic expertise, and robust tools to help our clients deliver life-changingtherapies to market. you take ownership, anticipate problems, find solutions and deliver results. you take ownership, anticipate problems, find solutions and deliver results; coordinating the activities of clinical management members which are allocated to a project on a regional or country basis. you will work in partnership with the project manager to ensure the necessary training, tracking and quality systems are in place for the clinical management team and be primarily responsible for the clinical deliverables of the project within agreed timelines and budget. clinical team managers p...
**reporting to**:south europe em - agribusiness sales manager** the life sciences group of thermo fisher scientific currently has a vacancy for a sr. tss to lead the agribusiness commercial strategy in middle east. **position: agribusiness sr. tss middle east** **territory: middle east & turkey** **location**:dubai - uae/riyadh - saudi arabia language requirements: proficient english & arabic. **purpose**: drive the thermo fisher agribusiness commercial strategy in middle east & turkey.be responsible to achieve high motivation of every individual resulting in a best performing team to support the sales and support agribusiness emea team to achieve the financial targets. **major responsibilities** - achieve sales targets, both quarterly and annually. - develop and implement a strategy that leads to increased customer value creation and market share gain specific to each geography. - maintains and develops customer relationships at senior level - gathers, analyses and delivers information from the regions to allow the company to develop strategies and products appropriate to the market. - identifies, nurtures and focuses on key accounts and key opinion leaders to build mid long term growing strategy. - identifies competitor activities and develops tactical activities - distributor management - manage and build with high accuracy funnel and forecast process according to company standard **skills/experience required** sales accumen - develops and implements effective regional sales strategies in collaboration with regional teams with ability to work...
Job description our project delivery team advises, coordinates, and manages the technical and operational aspects of projects, securing the successful completion of clinical trials. we collaborate with functional area leads to identify and evaluate fundamental issues on the project and ensure that solutions are implemented. the business segment lead is accountable for establishing and ensuring successful completion of assigned biopharma hematology/oncology studies/portfolio/clients through the oversight of relevant resources/functions. - accountable for achieving overall financial goals (sales/repeat business, revenue, and profitability). - works globally with other groups to develop new and/or support existing biopharma business. - collaborates with leadership in all functional areas on the continuous development/improvement of business processes to support cross functional teams and to ensure that work is uniform, complete, and led appropriately. this role lead and oversee work for global biopharma clients to drive therapeutic area strategies to ensure optimum performance. key responsibilities include: - ensures the timely execution of clinical trials with a focus on quality deliverables and profitability. - responsible for and ensures proactive identification of project risks and potential contingencies impacting time/quality/cost of deliverables are effectively handled and raised through appropriate escalation pathways. - further assesses all risks for potential impact across multiple projects and any cross therapeutic impact. - reviews and assesses proje...
**work schedule** standard (mon-fri) **environmental conditions** office **are you an ambitious professional seeking to excel in a dynamic sales environment? thermo fisher scientific inc., a world-class leader in serving science, is looking for a dedicated account manager iii to join our team in colombia. this is an outstanding opportunity to contribute to a company that makes a global impact on health, safety, and the environment.**: **responsibilities**: - successfully implement and manage key and strategic accounts within the colombian market. - develop and implement ambitious strategies to drive growth and maintain a top clinical market share. - collaborate with internal teams to deliver flawless service and support to clinical and research customers. - cultivate and uphold positive relationships with key clients to understand their needs and offer tailored solutions. - strictly adhere to company policies and ethical standards while competing in the marketplace. **requirements**: - proven experience in sales, specifically within the laboratory equipment, consumables, or biotechnology sectors. - comprehensive understanding of the colombian market and its outstanding dynamics. - outstanding communication and negotiation skills to effectively manage customer relationships. - ability to build, develop, and implement strategies that align with company objectives. - demonstrated ability to work both independently and as part of a collaborative team to achieve goals....
Summarized purpose: provides administrative and technical support to the project team. supports audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's sop and department guidance document. provides administrative support for site activation activities. aids the development of the critical path for site activation within assigned projects in support of rapid site activations. represents crg personnel. may utilize local knowledge, organization systems, external site lists and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. may act as a buddy during onboarding phase and provide training to new staff as needed. essential functions: according to the specific role (central or local), coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix. performs department, internal, country and investigator file reviews as assigned, and documents findings in appropriate system(s). ensures allocated tasks are performed on time, within budget and to a highquality standard. proactively communicates any risks to project leads. provides system support (, activate & etmf) and ensures system databases are always current. performs administrative tasks on assigned trials, including, but not limited to, timely processing of documents sent to client (e)tmf as assigned, performing (e)tmf reviews, distributing mass mailings and communications as needed, providing documents and ...
Summarized purpose: performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ich gcp, fda guidelines, local regulations and ppd sops. conducts site visits to assess protocol and regulatory compliance and manages required documentation. ensures that data will pass international quality assurance audits. represents ppd in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel. may assist project manager or clinical team manager on assigned projects. generally required to travel 60-80% but more for some individuals. essential functions and other job information: monitors investigator sites to ensure the accuracy and validity of crf entries in functions relation to patient records/clinic notes (source document verification). assess investigational product through physical inventory and records review. documents observations in reports and letters in a timely manner using approved business writing standards. escalates observed deficiencies and issues to clinical management expeditiously, proposes solutions and follow all issues through to resolution. maintains regular contact between monitoring visits with investigative sites to prove that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. conducts monitoring tasks in accordance with the approved monitoring plan. provides trial status tracking and progress update reports to the clinical team man...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. we are seeking a in our global clinical supplies team (based serbia or bulgaria ). the role can be fully homebased (or office, hybrid in sofia or belgrade) this role manages the full supply chain oversight for high complex global clinical trials. ensures project/study activities are in compliance with company and client requirements. mentors, trains and provides on-going support to junior team members. may act as main contact and escalation point for assigned clients. provides consultation services to clients and may develop and update client-specific manuals. builds and maintains client relationships. a day in the life develops study specific plans for each assigned project. meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/s...
(other duties may be assigned): • assist with implementing one or more of the following (under supervision): • development of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions. • program models using microsoft excel with visual basic for applications (vba). • conduct analyses and presentation of results. • conduct literature reviews with emphasis on extracting data pertinent to health economic evaluations and cost-effectiveness analyses. • conduct basic statistical analyses (, descriptive statistics and regression analysis). • assist with drafting sections of project deliverables (, user guides, model specifications and technical reports). • participate in client meetings and draft meeting minutes. • assist with tracking budget and expenses and monitoring timelines and deliverables for projects when assigned. • support other "non-billable" activities as needed (, assist with developing sections of proposals). • travel may be required. education, professional skills & experience: • master’s degree in operations research or industrial engineering or bachelor’s degree in operations research or industrial engineering with more than one year of relevant work experience. • master’s or bachelor’s degrees in other fields will be considered (, mathematics, economics, epidemiology) with relevant experience of programming decision analytic models (, decision trees, markov, individual state-transition, survival partition) in microsoft excel with vba. computer skills • required: excel and vba ex...
• coordinates, supports and performs administrative work to support the department. • supports the day to day operations of the study drug, comparators and ancillaries management. • supports department project teams as assigned member. • completes role specific training compliance and timesheets completion and release. • may coordinate or serve as a liason cross-functionally. • executes import & export activities according to ppd requirements, client requirements and applicable regulations. • executes the import & export / trade compliance plan for each project assigned. • meet with the trade compliance manager to discuss import & export issues. provides appropriate recommendations and alerts. • participates in ongoing training on new regulations concerning import/exports activities. • maintain updated ppd owned metrics indicators reports. • works under supervision and on low complexity trials....
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. our global clinical operations colleagues within our ppd clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies. discover impactful work: performs and coordinates all aspects of the clinical monitoring and site management process. conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. manages procedures and guidelines from different sponsors and/or monitoring environments ( fso, fsp, government, etc.). acts as a site processes specialist, ensuring that the trial is con...
Work schedule standard (mon-fri) environmental conditions office job description here’s what you’ll do: - works with global regulatory lead(s), regulatory strategists, global regulatory sub-teams and project teams regarding the development and execution of regulatory strategy through the product development lifecycle. - coordinate, develop and contribute to content and format of regulatory submissions and related supplements and amendments, including fda meeting requests, briefing books, inds, ctas, pediatric plans, dsurs, maa/bla/nda, etc. - identify and assess regulatory risks for assigned projects or programs. - senior manager may serve as point of contact with regulatory agencies relevant to assigned projects or programs, as appropriate. - ability to work both independently and within project teams, committees, etc. to achieve group goals. - accountable for tracking, following up and archiving correspondence, regulatory commitments, and queries from health agencies here’s what you’ll bring to the table: - ba/bs degree in a scientific/engineering/healthcare discipline required, masters, pharmd or phd preferred. - 5+ years of experience in the pharmaceutical industry preferred in latam countries. - 3+ years of experience in regulatory strategy or relevant training/experience preferred - experience in infectious diseases and/or biologicals is preferred - strong knowledge of current us and eu regulations - strong experience with ctd format and content of regulatory filings - exceptional written and oral communication in english and spanish. - knowl...
We are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. our **global clinical supplies** team cover all aspects from purchasing to global inventory management and from distribution to destruction. we have a new vacancy for **project manager/senior project manager** (depending on experience) for our **global clinical supplies team** to be based in the **latam** **region**. this can be office based or home based. **key responsibilities**: a project manager (pm) in the gcs team is responsible for providing overall global coordination of the entire clinical supplies lifecycle for the projects assigned. also responsible for managing the more complex clinical supplies studies. these studies require primary and/or secondary packaging and labelling design, drug projections, drug distribution and returns, drug inventory management, budgeting and developing project specific material for multiple projects at the same time. the pm provides consultation services to clients regarding global packaging, labelling, and distribution requirements. this person also serves as the main point of contact between the client, clinical project teams, third party vendors, and study sites. **education and experience**: - bachelor's degree in a science or related disci...
Ppd is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. at ppd, we are passionate, deliberate, and driven by our purpose - to improve health! - our colleagues in corporate strive for excellence in every task, at every moment. we are game changers seeking improvements to processes and more efficient ways of working or adapting to changing financial and industry environments. - as an administrative assistant at ppd you will provide support in the day to day administrative functions such as scheduling meetings, completing expense reports, and coordinating travel. - at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. - summarized purpose: - provides administrative support performing the day-to-day administrative functions including planning, organizing and scheduling. - essential functions: - inventories, orders and distributes office supplies. - sorts and distributes incoming mail, correspondence and other printed material. - sets up, organizes and maintains correspondence files and other departmental records. - arranges travel schedule and reservations and prepares expense reports and ensures submission in a timely fashion. - assists in preparation of presentations by compiling and preparing materials as needed. - coordinates details of onsite and offsite meetings and confere...
We are looking for a research associate iii (senior health economist - heor) to implement simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. manage multiple projects with tasks varying to degree by project. responsible for assisting the principal investigator with project management scoping, tracking progress, and delegating tasks to the project teams working on multiple projects. you will also: - implement one or more of the following with guidance from the principal investigator: - design and development of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions. - program the models using microsoft excel with visual basic for applications (vba) or simulation specialized software (e.g., arena) and conduct model validations. - conduct literature reviews with emphasis on extracting data pertinent to health economic evaluations and cost-effectiveness analyses. - conduct basic statistical analyses (e.g., descriptive statistics and regression analysis) - support development and maintenance of scientific resources (e.g., model templates, modeling training manuals). - draft project deliverables (e.g., excel with vba based models, user guides, model specifications and technical reports) and draft abstracts and sections of manuscripts with possible co-authorship. - responsible for developing a project plan and monitoring project progress (budget, timelines an...
**work schedule** other **environmental conditions** office join our dynamic team at thermofisher, a leading global organization dedicated to delivering excellence in logistics solutions across the latin american region. with a focus on innovation, efficiency, and customer happiness, we strive to optimize supply chain operations and drive growth for our clients. **key responsibilities**: **supply chain management**: coordinate end-to-end logistics processes, including transportation, warehousing, and inventory management, to ensure timely and efficient delivery of goods. **customs compliance**: ensure compliance with customs regulations and documentation requirements for international shipments, including import/export documentation and tariff classifications. **process improvement**: identify opportunities for process improvement and implement best practices to enhance efficiency, reduce costs, and streamline operations. **data analysis**: utilize data analytics tools to supervise key performance indicators (kpis), analyze trends, and generate insights to advise decision-making and drive continuous improvement. **cross-functional collaboration**: collaborate closely with internal stakeholders, including sales, procurement, and customer service teams, to align logistics strategies with business objectives and customer requirements. **qualifications**: - bachelor's degree in logistics, business administration or a related field. - 4+ years of experience in logistics import operations in a multinational or regional context. - strong understanding of t...
Supports supply chain for moderate complex global clinical trials. ensures project/study activities are in compliance with company and client requirements. may act as a representative and project lead for the department on less complex projects. - develops study specific plans for each assigned project. - meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets. - ensures fluent communication and interaction between internal departments in order to avoid obstacles during the course of the study. - integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with gxp requirements. - participates in ongoing training on new regulations....
Ppd’s mission is to improve health. it starts as an idea to find a cure. it becomes a life saved. all in-between, it’s you! we know that meaningful results not only require the right approach, but also the right people. we invite you to re-imagine health promoting protocols with us, working alongside our hardworking, bright and energetic teams. from purchasing to global inventory management and from distribution to destruction, ppd’s integrated global clinical supplies (gcs) services are designed to increase speed and efficiency, without sacrificing the quality you expect. as a project manager in clinical supplies, you will be r esponsible for providing overall global coordination of the entire clinical supplies lifecycle for the projects assigned. responsible for leading the more complex clinical supplies studies. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. summarized purpose: responsible for providing overall global coordination of the entire clinical supplies lifecycle for the projects assigned. responsible for running the more complex clinical supplies studies. these studies require primary and/or secondary packaging and labeling design, drug projections, drug distribution and returns, drug inventory management, budgeting and developing project specific material for multiple projects at the same time. provides consultation services to clients regarding global packaging, la...
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