**location/division specific information** we are looking for this position in méxico, chile, colombia or brazil. **how will you make an impact? (objective)** **what will you do? (responsibilities)** - a strategic sales plan for all direct and indirect markets with the latam region with key milestones in place - achieve/exceed revenue plan for each country within latam. - defend, win back, and grow share in latam. - develop an aligned and focused sales team with clear accountability, ownership, and implementation of sales best practices - create, implement, and develop a strong sales infrastructure inclusive of crm, business intelligence, and activity management - develop a detailed strategy for the top ten accounts in latam - driving growth in the emerging markets - point person to represent hid in latam with key internal and external stakeholders - strong relationships with strategic partners, kols, influencers and other working groups - excellent relationships with the global hid team (sales, product management, & marketing) - predictable revenue quarters with strong year over year growth - understand distributor relationships and influence changes where needed - design and implement robust revenue forecasting process and gain compliance by all regions in latam to adhere to this process - leading the hid team to conform to all of the ethical standards set by thermo fisher scientific. - driving our dealers, distributors and business partners to conform to all of the ethical standards set by thermo fisher scientific **how will you get here?** **edu...
**health economics modeler - evidera** - **we are looking to fill this role in colombia (fully remote)** **_ evidera’s modeling and simulation team is one of the largest and most experienced in-house team of modelers. evidera has designed, developed, and implemented hundreds of health economic and other models in all major therapeutic indications and for all major markets. we have an impressive track record of quality work and driving innovation, this along with the strength and tenure of our leadership team has given us a pre-eminent position in the market._** **position overview**: assist with implementing 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. assist with scientific and financial project management, and monitoring progress for projects when assigned. **essential duties and responsibilities (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 (e.g., descriptive statistics and regression analysis). - assist ...
**senior health economist modeler (sra), evidera modeling & simulation** **we are looking to fill this role in us, canada, uk or eu & are **flexible to fully remote work** this is a great time to join this rapidly expanding global modeling team! - ** our senior team members have the flexibility to focus on scientific, management or commercial career tracks.**: - **we also offer customizable cross-training opportunities for those interested in broadening their experience across evidera’s teams.** our multidisciplinary modeling & simulation experts design & implement health economic models to: - describe complex medical processes - understand and evaluate the implications of clinical trials - demonstrate the value of interventions beyond efficacy - assess benefits, risks, and the economic consequences associated with healthcare interventions. typical projects include health economic modeling to conduct cost-effectiveness analyses of healthcare interventions and implementing decision-analytic models (e.g., decision trees, markov, individual state transition, survival partition), research and data analytics. **position overview**: - conceptualization, design and implementation of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions - as co-principal investigator: project budget, deliverable, resourcing and timeline responsibility; identify scope expansion and need for amendments - assumes responsibility for sales targets and building client relationships. **essential duties and responsibilities (othe...
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 conferences in...
**work schedule** standard (mon-fri) **environmental conditions** office **qualifications**: education and experience: high / secondary school diploma or equivalent and relevant formal academic / vocational qualification. bachelor's degree preferred. previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year). in some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. k**nowledge, skills and abilities**: - ability to work in a team or independently as required. - good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively. - demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency. - strong customer focus. - flexibility to reprioritize workload to meet changing project timelines. - demonstrated ability to attain and maintain a good working knowledge of applicable country regulations, ich good clinical practices, and organization/client sops and wpds for all nonclinical/clinical aspects of project implementation, execution and closeout. - good english language and grammar skills and proficient local language skills as needed. - good computer skills, proficient in ms office (word, excel, and powerpoint) and ability to obtain knowledge and master all clinical trial database systems. - ability to successfully complete ...
A senior vendor management coordinator provides supply chain oversight for third party vendors. selects and contracts with appropriate vendors for scope of client's study. provides complete oversight of vendor supply chain for high complexity global clinical trials in multiple regions. provides financial control and oversight of pass-through budgets. ensures that vendors execute activities in accordance with contracted strategy. maintains close collaboration of i/e activities to ensure that appropriate regulations are followed for all countries imports and exports. acts as a representative for the vendor management department on all assigned projects. sets vendor strategy with external partners for procurement and depot vendors for particular clients. collaborates with vendors to improve processes and improve supply chain oversight, delivers trainings to vendor management team. mentors and provides guidance to junior members of the vendor management team....
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...
**work schedule** standard (mon-fri) **environmental conditions** office **responsabilidades primarias** iniciar proceso de alta de los productos y clientes requeridos en la herramienta eagle (mdm) preparar, procesar y realizar un seguimiento de las cotizaciones solicitadas por el área comercial y/o solicitudes directas de los clientes procesar en nuestro erp (jde) las ordenes de compra de los clientes y notificar la recepción de esta indicando el folio interno con el que ha quedado registrado asegurarnos sea detonada la compra de los materiales que se amparen en la oc proporciona seguimiento a las órdenes de compra de los clientes hasta la entrega final. informar al cliente sobre el estado de los pedidos. gestión y administración los materiales en stock y cumplir con las entregas y envíos programados de acuerdo con los horarios del cliente. realizar seguimiento del informe de pedidos abiertos (backlog) frente a los materiales disponibles en el almacén de las cuentas de clientes asignadas para programar el envío con logística responde y aborda eficazmente todas las consultas y solicitudes de los clientes. atiende las llamadas de los clientes para solicitar cotizaciones, quejas, estado del pedido, información sobre el tiempo de entrega, servicio y soporte técnico; canalizar al área responsable según corresponda. gestión y correcta administración de los buzones de correo electrónico (bandeja de customer service y correo individual) a través de nuestro crm (right now) contribuir en el logro de nuestros objetivos, mensuales y anuales; atención ...
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 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: acts as the lead data manager for one or more projects or to provide support to the lead data manager. may lead all data management activities for individual, limited volume/complexity studies with ...
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 manager clinical data management, you will help ensure the success of your team and cdm projects. you will work to provide training, mentorship and guideance. this includes but not limited to interviewing new staff, performance management, reviewing and approving time and expense reports. 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: manages project staff and workload of direct reports. responsible for training, mentoring, and guiding project staff and direct reports within a portfolio. essential functions: - manages staff, which may include int...
**work schedule** other **environmental conditions** office are you ready to launch your career in the financial industry? thermo fisher scientific inc. is offering a unique opportunity for an individual who consistently demonstrates exceptional work behaviors to join our world-class team as an finance intern. as a global leader in serving science, we are dedicated to making the world healthier, cleaner, and safer. here's your chance to be a part of our ambitious mission and contribute to scientific advancements that impact lives globally. **location**: bogotá colombia **responsibilities**: - assist in financial analysis and reporting - support budgeting and forecasting processes - research current financial trends and effective strategies - collaborate with cross-functional teams to determine financial strategies - prepare and present financial reports to senior management **requirements**: - bachelor's degree in finance or related field, or equivalent experience - proven knowledge of financial principles and concepts - strong analytical and problem-solving skills - excellent attention to detail and ability to deliver flawless work - ability to compete in a fast-paced and dynamic environment at thermo fisher scientific, we value inclusion and collaboration. our diverse team of over 100,000 colleagues shares a common set of values - integrity, intensity, innovation, and involvement. we are committed to providing equal opportunity employment and fostering an environment where diverse experiences, backgrounds, and perspectives are celebrated and va...
**summarized purpose**: performs and coordinates different aspects of the clinical monitoring and site management process. **essential functions** - monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (rca), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into - compliance and decrease risks. ensures data accuracy through sdr, sdv and crf review as applicable through on-site and remote monitoring activities. - 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 and follow all issues through to resolution. - may need to maintain regular contact between monitoring visits with investigative sites to confirm 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. participates in the investigator payment process. ensures a - shared responsibility with other project team members on issues/findings resolution. investigates and follows-up on findings as applicable. - participates in investigator meetings as necessary. may help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. initiates ...
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 manager clinical data management, you will help ensure the success of your team and cdm projects. you will work to provide training, mentorship and guideance. this includes but not limited to interviewing new staff, performance management, reviewing and approving time and expense reports.at ppd we hire the best, develop ourselves and each other, and recognize the power of being one te...
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 conferences in...
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. - knowledge of and broad ...
Are you a problem solver who loves challenges and enjoys creativity? we have an exciting opportunity for a master data analyst on our quality analytics & reporting team within quality risk management. we need someone who is driven to deliver results and has strong and proactive communication skills. as an analytics expert, you will not only facilitate delivery of insights to multiple businesses but will take an active role in identification of root causes to prevent and eliminate recurring issues. as a master data analyst, you will lead projects to design and create complex reports and dashboards, and analyze data using advanced statistical analysis tools and techniques. you will direct and mentor junior staff to develop, validate, and deliver high-quality analytics to enhance the quality of our clinical trials. don't miss this opportunity to join us at thermo fisher scientific, where we are seeking to improve our customers' experience while driving technology solutions to solve the world's scientific problems! **what will you do?** - collaborate with quality business partners to understand and support their analytical needs and deliver useful insights to relevant decision-makers. - design, develop & enhance global reports and dashboards. build and maintain innovative interactive visualizations through data interpretation and analysis, integrating various reporting components from multiple data sources. - statistically analyze data to answer key questions from business partners or out of self-initiated curiosity with an eye for what drives business performance, investi...
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 manage 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 scopes include: infectious and respiratory diseases, oncology/hematology, neurosciences, cardiovascular and metabolic, general medicine and vaccines. **discover ...
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....
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 distributed team, you may engage in diverse initiatives and projects, or be part of a virtual international project team gaining cross-cultural experience. therapeutic scopes include: infectious and respiratory diseases, oncology/hematology, neurosciences, cardiovascular and metabolic, general medicine and vaccines. **discov...
Specific responsibilities: - lead the negotiating and drafting of strategic agreements with key accounts, channel partners and vendors; - act as primary point of contact for multiple client groups within the company, leveraging internal and external resources to timely and cost-effectively meet the legal needs of client groups; - provide primary legal support on contracts process, a heavy workload of contractual matters, refine contracts processes and provide trainings; - collaborate with commercial, operations and regulatory departments on various projects including development of new business models in new territories of the region; - manage outside counsels in central region; - collaborate with colleagues in other latam countries, us, europe and apac exchanging experiences; - provide ad hoc legal support on special projects as needed. qualifications / requirements: - fluent english are required (speaking, listening and writing, including technical writing for contracts and notifications). portuguese language skills are desirable; - strong organizational, analytical and problem-solving skills; - ability to effectively evaluate legal exposure, manage risk and develop creative, client-focused solutions to achieve business goals within appropriate legal guidelines; - draft, review and negotiate a wide range of contracts, identifying and prioritizing high-risk and mission critical transactions; - ability to work in a fast-paced environment with multiple competing deadlines, leveraging internal and external resources to meet multiple simultaneous deadlines; - ...
Description - external 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 talented, 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. a procurement and logistics executive provides support to clinical supplies operations and administrative activities in all areas of clinical supplies lifecycle of low to moderate complexity studies. **activities** - actively participates in global project calls and lead discussions on assigned supply chains and liaises with global supply vendors. - makes global purchases, global distributions and deposit processes. - oversees post-sale services and process distribution. - must poses a solid understanding of the clinical supply process, such as manufacturing, handling, importing, shipping, exporting, auditing, labeling, and packaging - ensures all activities are executed in compliance with company good practices and client requirements. qualifications - external **requirements**: - bachelor degree - advanced english and good communication skills both written and verbal - proficient in microsoft office programs - strong customer service orientation and attention t...
**summarized purpose**: performs and coordinates different aspects of the clinical monitoring and site management process. **essential functions** - monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (rca), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into - compliance and decrease risks. ensures data accuracy through sdr, sdv and crf review as applicable through on-site and remote monitoring activities. - 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 and follow all issues through to resolution. - may need to maintain regular contact between monitoring visits with investigative sites to confirm 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. participates in the investigator payment process. ensures a - shared responsibility with other project team members on issues/findings resolution. investigates and follows-up on findings as applicable. - participates in investigator meetings as necessary. may help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. initiates ...
**job title: logistic specialist (latam)** **company overview**: 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 tr...
A senior vendor management coordinator provides supply chain oversight for third party vendors. selects and contracts with appropriate vendors for scope of client's study. provides complete oversight of vendor supply chain for high complexity global clinical trials in multiple regions. provides financial control and oversight of pass-through budgets. ensures that vendors execute activities in accordance with contracted strategy. maintains close collaboration of i/e activities to ensure that appropriate regulations are followed for all countries imports and exports. acts as a representative for the vendor management department on all assigned projects. sets vendor strategy with external partners for procurement and depot vendors for particular clients. collaborates with vendors to improve processes and improve supply chain oversight, delivers trainings to vendor management team. mentors and provides guidance to junior members of the vendor management team....
Job description we are currently seeking a senior regulatory affairs specialist to join our global regulatory affairs department. this is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting. in this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (phase 1 to 4) clinical trials, studies and projects. you will be part of a global team providing innovative solutions and global regulatory expertise, being client interfacing to provide strategic regulatory intelligence and guidance. you will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients. you will act as a representative of the regulatory department with other departments, supporting business development, working on initiatives, and contributing to quality improvement. you will also arrange, lead, and report on client and regulatory agency meetings. the following skills are required to be successful in this position: - preparation and assembly of global regulatory submissions - interacting with sponsors, - review and assess clinical trial regulatory documents, - review and assess scientific literature. - manages project teams and preparation - participate in launch meetings, review meetings and project team meetings. optional skills: - experience with bid defense meetings **qualifications - external** wh...
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