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 ...
Performs and coordinates all activities required to finalize site contracts (including, contractual terms and conditions, associated investigator grant budget(s) payment schedule terms and conditions, ancillary and site-specific documents), with investigator sites, pharmacies, laboratories or other relevant contractual parties during the lifecycle of the study. reviews ppd and/or client site contract, budget, payment schedule and ancillary documents templates for compliance with local legislation and practices. adapts the site contract template to client and investigational site requirements in collaboration with key stakeholders to include the project team and the ppd legal team. facilitates effective budget negotiation with site personnel in collaboration with key stakeholders. performs and coordinates all amendments to site contracts and financial agreements with investigator sites, pharmacies, laboratories or other relevant contractual parties during the lifecycle of the study. serves as contact with investigative sites for contractual issues and negotiations throughout the lifecycle of a study. assumes responsibility for any ongoing contract or budget amendments....
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 ...
Join to apply for the logistics specialist i role at thermo fisher scientific join to apply for the logistics specialist i role at thermo fisher scientific work schedule standard (mon-fri) environmental conditions office logistics specialist i join thermo fisher scientific inc. and excel in an exceptionally dynamic role as a logistics specialist i in bogota. this position offers a fantastic opportunity to collaborate with a world-class team and successfully implement logistics operations critical to advancing clinical projects. responsibilities coordinate product receipts from the arrival at our facilities until release in the gpm system. process medication and supply orders to medical facilities and request receipt acknowledgments. collaborate on new project initiations and coordinate with medical centers for shipment and return of materials. generate administrative starts for projects, crafting necessary folders and forms. monitor material transfer processes and request final product disposals. advise medical centers on shipment procedures, storage conditions, and documentation. detect and report deviations, complete investigations, and propose process improvements. collaborate in reception, dispatch, and return processes, ensuring deadlines are met. perform monthly service registrations, attend to comments, and ensure timely registration. develop metrics for suppliers, performance indicators, and reports for customers. complete all activities efficiently and safely. requirements bachelor's degree in engineering, logistics operatio...
**location/specific division**: cali, colombia. **how will you impact your position (objective)**: develop and implement the strategies given by the management, for the growth of the assigned area, promoting, negotiating, and acting as a factor of change in the different customers through tmf's solutions. driving the sales of solutions that are in line with the objectives set in advance for the area, also requires someone who has in his dna the core values of tmf (integrity, involvement, intensity, innovation, etc.).) **what will you do (responsibilities)**: - focus on clinical, academic, and f&b; markets. - perform frequent meetings face-to-face and virtual with or without tss. - identify key customers and secondary customers. - craft a sales plan for each type of customer. - build funnel pipeline and join forecast calls - analyze sales results and market trends. - identify customer’s needs and be able to propose a solution with a biotechnology portfolio. - work together with functional areas to ensure the best customer experience as marketing, service and support, regulatory affairs, customer care, supply chain, distribution, etc). - identify stock for assigned customers. **how do you get there?** **education requirements**: - biological graduation (biology, pharmacy, biomedical, chemistry, etc), preferably with master in the same area or sales. - english fluence (writing and speaking). - 50% travel availability. **experience (technical knowledge/expertise)**: - 3-4 years of commercial experience. **knowledge, skills, and proficiencies**: ...
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...
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 have an opportunity to join our best in class global feasibility group as an associate feasibility strategist, a senior level position within the team. the role sources and analyzes data to develop site and patient strategies for proposals and post-award feasibility offerings. you will handle pre-award efforts and post-award trial optimization and/or site id assessments. your scope starts at the request for proposal stage through to the end of the feasibility assessment, delivering accurate and robust data-driven strategies to drive a successful study endpoint. travel requirements for the role include attending bid defense meetings once quarterly. essential duties: - develops and presents strategies to clients using modeling tools that mine and aggregate data sources and ...
Basic medical/therapeutic area knowledge and understanding of medical terminology - ability to attain and maintain a working knowledge of ich gcp, applicable regulations and crg procedural documents - effective oral and written communication skills - excellent interpersonal and customer service skills - good organizational and time management skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively - proven flexibility and adaptability - ability to work in a team or independently, as required - well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving - proficient computer skills with good knowledge of ms office ability to learn and use appropriate software. leverage modern technology when applicable - ability to extract pertinent information from all study documents, electronic study data systems, ctms and dashboards - excellent english language and grammar skills...
Roles and responsibilities for the overall success of the proposal development process within the **general medicine** team space; from rfp receipt through client decision. provides leadership and ownership of operational strategies, bid defense hand=off, and accountability for all related operational proposal deliverables, resulting in an increased rfp hit rate, and positive business growth. leverages all opportunities to achieve targets while enhancing customer relations. primarily responsible for rfps and supplemental documents for complex, multi-region, multi-service clinical development projects/programs, partnership and prospective selling initiatives and related client deliverables. converts commercial win strategy into operational strategy that maximizes rfp hit rate resulting in business growth for gen med; determines the level of proposal deliverable and key operations messages and supports the triage process within clinical operations to meet proposal deliverables. ensures budget reflects operational strategy and manages operations proposal deliverable in order to achieve ppd profitability targets. collaborates with therapeutic and cross functional leadership team to assess success and profitability and ability to execute to plan, assessing process and bidding algorithms. drives the development of the operations segment of the proposal deliverable within prescribed timelines, disseminates operational strategy to proposal team and develops kpi's, ensuring a successful operations segment of the deliverable. partners with clinical operations, commercial or...
**summarized purpose**: **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. - provides trial status tracking and progress update reports to the clinical team. - manager (ctm) as required. ensures study systems are updated per agreed study conventions (e.g. clinical trial management system, ctms). performs qc check of reports generated from ctms system where required. - participates in in...
**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 (i.e., 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 n...
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 ...
Join to apply for the logistics specialist i role at thermo fisher scientific join to apply for the logistics specialist i role at thermo fisher scientific work schedule standard (mon-fri) environmental conditions office logistics specialist i join thermo fisher scientific inc. and excel in an exceptionally dynamic role as a logistics specialist i in bogota. this position offers a fantastic opportunity to collaborate with a world-class team and successfully implement logistics operations critical to advancing clinical projects. responsibilities - coordinate product receipts from the arrival at our facilities until release in the gpm system. - process medication and supply orders to medical facilities and request receipt acknowledgments. - collaborate on new project initiations and coordinate with medical centers for shipment and return of materials. - generate administrative starts for projects, crafting necessary folders and forms. - monitor material transfer processes and request final product disposals. - advise medical centers on shipment procedures, storage conditions, and documentation. - detect and report deviations, complete investigations, and propose process improvements. - collaborate in reception, dispatch, and return processes, ensuring deadlines are met. - perform monthly service registrations, attend to comments, and ensure timely registration. - develop metrics for suppliers, performance indicators, and reports for customers. - complete all activities efficiently and safely. requirements - bachelor's degree in engineering, logistics operati...
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 ...
**work schedule** other **environmental conditions** office 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 currently seeking a senior regulatory affairs specialist to join our global regulatory affairs department - **regulatory science** team. 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 ad...
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 pharmacovigilance department. specifically in relation to submissions, tracking and subsequent filing and archiving or expedited and periodic safety reports. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to safety reporting. may mentor or train new central safety reporting admin staff. a day in the life: •responsible for the submission of safety reports to applicable parties, including subsequent scanning, indexing and filing (both electronic and paper), safety tracker completion and quality check, and archiving in accordance with sop’s and wpd’s. resolves simple problems with submission packs within minimal inp...
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. essential functions receives, prepares and submits safety reports to applicable parties. ensures that all reports are compliant with regulatory timelines and country legislation and monitors this on a regular basis. leads large scale projects effectively, ensuring safety reports are submitted in accordance with the agreed processes and regulatory timelines. provides input and feedback to aid the development of program and departmental procedural documents. shares ideas and suggestions with team members. takes an active role in the development and implementation of ideas and suggestions. liaises with relevant departments around safety reporting tasks and attends various meetings as required. provides input, feedback and guidance to other team members and mentors new starters. ...
Work schedule standard (mon-fri) environmental conditions office job description logistics specialist i join thermo fisher scientific inc. and excel in an exceptionally dynamic role as a logistics specialist i in bogota. this position offers a fantastic opportunity to collaborate with a world-class team and successfully implement logistics operations critical to advancing clinical projects. responsibilities coordinate product receipts from the arrival at our facilities until release in the gpm system. process medication and supply orders to medical facilities and request receipt acknowledgments. collaborate on new project initiations and coordinate with medical centers for shipment and return of materials. generate administrative starts for projects, crafting necessary folders and forms. monitor material transfer processes and request final product disposals. advise medical centers on shipment procedures, storage conditions, and documentation. detect and report deviations, complete investigations, and propose process improvements. collaborate in reception, dispatch, and return processes, ensuring deadlines are met. perform monthly service registrations, attend to comments, and ensure timely registration. develop metrics for suppliers, performance indicators, and reports for customers. complete all activities efficiently and safely. requirements bachelor's degree in engineering, logistics operations, health areas, administration, or related fields. at least one year of experience in similar tasks within the pharmaceutical industry or logistics companies. knowledge of gxp sta...
Work schedule standard (mon-fri) environmental conditions office job description 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 pharmacovigilance department. specifically in relation to submissions, tracking and subsequent filing and archiving or expedited and periodic safety reports. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to safety reporting. may mentor or train new central safety reporting admin staff. a day in the life: • responsible for the submission of safety reports to applicable parties, including subsequent scanning, indexing and filing (both electronic and paper), safety tracker completion and quality check, and archiving in accordance with ...
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 seeking an individual with a track record of success in vendor management to join our world-class team of researchers. as a leader in the scientific industry, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer. responsibilities: collaborate with cross-functional teams to determine vendor requirements and establish sourcing strategies manage vendor relationships and contracts, ensuring flawless execution and delivery conduct market research and competitive analysis to identify potential vendors develop and implement vendor performance metrics and conduct regular evaluations drive continuous improvement initiatives to optimize vendor management processes requirements: bachelor's degree in business administration or related field, or equivalent experience in the industry. previous experience in vendor management or procurement strong analytical and negotiation skills excellent communication and interpersonal skills proven ability to successfully implement vendor management strategies at thermo fisher scientific, we value diversity and inclusivity. we believe that collaboration and different perspectives drive innovation and lead to exceptional results. we are an equal opportunity employer and strictly prohibit discrimination based on race, color, religion, sex, sexual orientation, gender identity,...
Join to apply for the proj mgr clin supplies role at thermo fisher scientific continue with google continue with google join to apply for the proj mgr clin supplies role at thermo fisher scientific work schedule standard (mon-fri) environmental conditions office 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. the role we are seeking an associate project/project manager to join our global clinical supplies team. this can be office based, hybrid, or fully homebased. a day in the life this role provides complete oversight of supply chain for sophisticated global clinical trials. ensures project/study activities are in compliance with company and client requirements and acts as a representative for the department on all assigned projects. key responsibilities: develops study specific plans for ...
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