job summary: The Senior Manager/ Associate Director, Engagement Platforms & reporting will support roadmap, implementation and maintenance of technology platforms and measurement reporting for Medical Engagement activities across company Global Medical Affairs (GMAF). He/she will support functional Medical Engagement Leads with platform implementation and ongoing maintenance with emphasis on field medical related-systems. Additionally, he/she will impleme
job summary: The Senior Manager/ Associate Director, Engagement Platforms & reporting will support roadmap, implementation and maintenance of technology platforms and measurement reporting for Medical Engagement activities across company Global Medical Affairs (GMAF). He/she will support functional Medical Engagement Leads with platform implementation and ongoing maintenance with emphasis on field medical related-systems. Additionally, he/she will impleme
job summary: Manager, Global Medical Affairs (IST Operations) 1 Year Contract (potential tor extend) Remote | EST Hours Join a leading biopharma team supporting the execution and oversight of Investigator Sponsored Trials (ISTs) within Global Medical Affairs. T his operations-focused role is ideal for a detail-oriented professional with 3+ years of industry experience and a strong background in Project Coordination, Resource Planning, and Cross-functional
job summary: Manager, Global Medical Affairs (IST Operations) 1 Year Contract (potential tor extend) Remote | EST Hours Join a leading biopharma team supporting the execution and oversight of Investigator Sponsored Trials (ISTs) within Global Medical Affairs. T his operations-focused role is ideal for a detail-oriented professional with 3+ years of industry experience and a strong background in Project Coordination, Resource Planning, and Cross-functional
job summary: Project Manager (Smartsheet Program Planner) - Medical Affairs Term & Timing: 1-year Contract beginning in January 2026 Are you a Smartsheet super user with a passion for driving operational excellence? We're looking for a Project Manager (Smartsheet Program Planner) to join a leading biotech - US Medical, Strategy & Operations team. You'll leverage your Smartsheet expertise to manage critical project plans and support key initiatives, acting
job summary: Project Manager (Smartsheet Program Planner) - Medical Affairs Term & Timing: 1-year Contract beginning in January 2026 Are you a Smartsheet super user with a passion for driving operational excellence? We're looking for a Project Manager (Smartsheet Program Planner) to join a leading biotech - US Medical, Strategy & Operations team. You'll leverage your Smartsheet expertise to manage critical project plans and support key initiatives, acting
job summary: Responsible for overseeing the design and delivery of trials within a given late phase program or multiple early-phase programs in the Immuno-Oncology group.Reports to the Medical Lead for the given program(s) and is accountable for defining the strategy and execution of assigned trials. Clinical team leader with clear understanding of areas of responsibilities and accountabilities of the role.Team player who is comfortable in situations
job summary: Responsible for overseeing the design and delivery of trials within a given late phase program or multiple early-phase programs in the Immuno-Oncology group.Reports to the Medical Lead for the given program(s) and is accountable for defining the strategy and execution of assigned trials. Clinical team leader with clear understanding of areas of responsibilities and accountabilities of the role.Team player who is comfortable in situations
job summary: Dive into a rewarding role as a Chemist I, where your passion for science and laboratory skills will make a direct impact. Working Wednesday-Saturday or Sunday-Wednesday, 2nd shift 4x10hr shifts, you'll be an essential part of a dynamic team, performing a variety of analytical chemistry tests within a Good Manufacturing Practices (GMP) environment. This is a unique opportunity to apply your expertise and attention to detail to ensure product
job summary: Dive into a rewarding role as a Chemist I, where your passion for science and laboratory skills will make a direct impact. Working Wednesday-Saturday or Sunday-Wednesday, 2nd shift 4x10hr shifts, you'll be an essential part of a dynamic team, performing a variety of analytical chemistry tests within a Good Manufacturing Practices (GMP) environment. This is a unique opportunity to apply your expertise and attention to detail to ensure product
job summary: Immediate openings for Bioprocess / Biomanufacturing Associates with a leading, global company focused on gene therapy innovation, located in the North Bay region of the Bay area. Position Type: 1 year contract, long term with potential for full time hire Schedule Alternating Tuesday/Wednesday, 6PM - 7AM. Starting on 10/5/25, the new work schedule will be Sunday - Tuesday and every other Saturday, 6 PM - 7AM (Sat/Sun - Tuesday). location
job summary: Immediate openings for Bioprocess / Biomanufacturing Associates with a leading, global company focused on gene therapy innovation, located in the North Bay region of the Bay area. Position Type: 1 year contract, long term with potential for full time hire Schedule Alternating Tuesday/Wednesday, 6PM - 7AM. Starting on 10/5/25, the new work schedule will be Sunday - Tuesday and every other Saturday, 6 PM - 7AM (Sat/Sun - Tuesday). location
job summary: In Company Thousand Oaks, the Automated Screening Platforms/ High-Throughput Assays group in the Lead Discovery & Characterization organization is seeking an entry-level temporary contract worker for a laboratory based on-site role to provide assay reagent preparation for screening assay delivery.The desired team member will primarily contribute to a high demand for routine cell culture (expansion, banking and quality-control) of various ma
job summary: In Company Thousand Oaks, the Automated Screening Platforms/ High-Throughput Assays group in the Lead Discovery & Characterization organization is seeking an entry-level temporary contract worker for a laboratory based on-site role to provide assay reagent preparation for screening assay delivery.The desired team member will primarily contribute to a high demand for routine cell culture (expansion, banking and quality-control) of various ma
job summary: Utilizing extensive clinical data management experience in study start-up, conduct, and closeout you will oversee the data management deliverables across assigned therapeutic area (TA) programs or projects, and partner with cross functional study teams and FSP. You will focus on timely quality delivery, as well as consistency across the Global Study Operations Data Management (GSO-DM) components. location: Telecommute job type: Contrac
job summary: Utilizing extensive clinical data management experience in study start-up, conduct, and closeout you will oversee the data management deliverables across assigned therapeutic area (TA) programs or projects, and partner with cross functional study teams and FSP. You will focus on timely quality delivery, as well as consistency across the Global Study Operations Data Management (GSO-DM) components. location: Telecommute job type: Contrac
job summary: Ready to leverage your expertise in medical review to shape promotional materials and drive strategic initiatives? We're seeking a Medical Reviewer/Safety Reviewer III to join our team on a contract basis. In this hybrid role based in Florham Park, NJ, you'll be instrumental in ensuring the accuracy and compliance of branded and unbranded content by providing crucial medical input throughout the Medical, Legal, and Regulatory (MLR) review pro
job summary: Ready to leverage your expertise in medical review to shape promotional materials and drive strategic initiatives? We're seeking a Medical Reviewer/Safety Reviewer III to join our team on a contract basis. In this hybrid role based in Florham Park, NJ, you'll be instrumental in ensuring the accuracy and compliance of branded and unbranded content by providing crucial medical input throughout the Medical, Legal, and Regulatory (MLR) review pro
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. As the world's leading provider of diagnostic information services, our client is committed to sharing our
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. As the world's leading provider of diagnostic information services, our client is committed to sharing our
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. As the world's leading provider of diagnostic information services, our client is committed to sharing our
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. As the world's leading provider of diagnostic information services, our client is committed to sharing our
job summary: This contract role for a Sr. Specialist, Drug Product QA is ideal for a meticulous quality assurance professional with a strong background in biotech or pharma, particularly in aseptic fill-finish operations. You'll be instrumental in ensuring GMP compliance, from reviewing and approving critical documentation and managing batch disposition to leading deviation investigations and providing on-the-floor QA guidance. This position offers a chan
job summary: This contract role for a Sr. Specialist, Drug Product QA is ideal for a meticulous quality assurance professional with a strong background in biotech or pharma, particularly in aseptic fill-finish operations. You'll be instrumental in ensuring GMP compliance, from reviewing and approving critical documentation and managing batch disposition to leading deviation investigations and providing on-the-floor QA guidance. This position offers a chan
job summary: Join a high-impact medical affairs team working on meaningful clinical and scientific initiatives that directly support product strategy, education, and commercialization. This remote opportunity is tied to a major biopharma company's North Chicago campus and offers the chance to lead key efforts in medical review, data dissemination, and scientific alignment across internal and external stakeholders. If you have experience in medical and pro
job summary: Join a high-impact medical affairs team working on meaningful clinical and scientific initiatives that directly support product strategy, education, and commercialization. This remote opportunity is tied to a major biopharma company's North Chicago campus and offers the chance to lead key efforts in medical review, data dissemination, and scientific alignment across internal and external stakeholders. If you have experience in medical and pro
job summary: As an experienced scientist, you will need to work independently and efficiently on Synthetic Biology including gene and oligo design, oligo synthesis, gene assembly, next generation sequencing and data analysis, nucleic acid purification and characterization, take lead in high throughput gene synthesis and plasmid production, process automation and protocol development, improvement of quality and throughput, problem solving etc. location:
job summary: As an experienced scientist, you will need to work independently and efficiently on Synthetic Biology including gene and oligo design, oligo synthesis, gene assembly, next generation sequencing and data analysis, nucleic acid purification and characterization, take lead in high throughput gene synthesis and plasmid production, process automation and protocol development, improvement of quality and throughput, problem solving etc. location:
job summary: Randstad is working with a world class partner in California and hiring for their Supply and Demand Planning Team, the Supply Planning Specialist will play a critical role in ensuring the availability of raw materials and finished goods to support manufacturing and distribution operations. This person will be responsible for balancing supply and demand, optimizing inventory levels, and collaborating cross-functionally to support business co
job summary: Randstad is working with a world class partner in California and hiring for their Supply and Demand Planning Team, the Supply Planning Specialist will play a critical role in ensuring the availability of raw materials and finished goods to support manufacturing and distribution operations. This person will be responsible for balancing supply and demand, optimizing inventory levels, and collaborating cross-functionally to support business co
job summary: Step into a pivotal Training Specialist/Developer role at the forefront of Clinical Trial Process Development and Delivery in a leading pharmaceutical company. This is a unique opportunity to directly shape and enhance global training initiatives, with a primary focus on developing cutting-edge eLearning content using Articulate Rise and Storyline. You'll work remotely, collaborating with process owners and functional leaders to build impactf
job summary: Step into a pivotal Training Specialist/Developer role at the forefront of Clinical Trial Process Development and Delivery in a leading pharmaceutical company. This is a unique opportunity to directly shape and enhance global training initiatives, with a primary focus on developing cutting-edge eLearning content using Articulate Rise and Storyline. You'll work remotely, collaborating with process owners and functional leaders to build impactf
job summary: Join a dynamic Quality Control team at a leading biopharmaceutical manufacturing site in Swiftwater, PA, where groundbreaking work in vaccine and biologics production is supported by rigorous quality systems. This is a full-time, onsite QC Analyst II role ideal for candidates with hands-on chemistry lab experience, especially in raw material and wet chemistry testing. You'll contribute directly to the safety and integrity of life-saving produ
job summary: Join a dynamic Quality Control team at a leading biopharmaceutical manufacturing site in Swiftwater, PA, where groundbreaking work in vaccine and biologics production is supported by rigorous quality systems. This is a full-time, onsite QC Analyst II role ideal for candidates with hands-on chemistry lab experience, especially in raw material and wet chemistry testing. You'll contribute directly to the safety and integrity of life-saving produ
job summary: Immediate opportunity for a Specialist Manufacturing, New Product Introduction. In this critical role, you will lead the introduction of new pharmaceutical products into the manufacturing plant in Thousand Oaks, CA. As a New Product Introduction (NPI) Lead, you will be responsible for cross-functional project management, change control ownership, and timeline execution to deliver clinical and commercial products into manufacturing right-firs
job summary: Immediate opportunity for a Specialist Manufacturing, New Product Introduction. In this critical role, you will lead the introduction of new pharmaceutical products into the manufacturing plant in Thousand Oaks, CA. As a New Product Introduction (NPI) Lead, you will be responsible for cross-functional project management, change control ownership, and timeline execution to deliver clinical and commercial products into manufacturing right-firs
job summary: Join a dynamic and fast-paced scientific environment at a leading R&D site in Waltham, MA, where innovation and collaboration drive global impact. As a Documentation Specialist, you'll play a key role in supporting the shipping and logistics process by ensuring regulatory compliance and precise documentation for outbound materials. This is an exciting opportunity for detail-oriented professionals eager to contribute to essential operations in
job summary: Join a dynamic and fast-paced scientific environment at a leading R&D site in Waltham, MA, where innovation and collaboration drive global impact. As a Documentation Specialist, you'll play a key role in supporting the shipping and logistics process by ensuring regulatory compliance and precise documentation for outbound materials. This is an exciting opportunity for detail-oriented professionals eager to contribute to essential operations in
job summary: Immediate opportunity for an R&D Analytical Chemist to contribute analytical and technical support for nitrosamines and impurities analysis. This individual will collaborate with subject matter experts (SMEs) to lead and execute laboratory experiments in support of renal therapy programs. This is a full-time, on-site position based in Round Lake, IL. The role is centered on LC-MS/MS analysis for the detection and quantification of impurities,
job summary: Immediate opportunity for an R&D Analytical Chemist to contribute analytical and technical support for nitrosamines and impurities analysis. This individual will collaborate with subject matter experts (SMEs) to lead and execute laboratory experiments in support of renal therapy programs. This is a full-time, on-site position based in Round Lake, IL. The role is centered on LC-MS/MS analysis for the detection and quantification of impurities,
job summary: Clinical Trial Liaison | 12 Month Engagement Are you a dynamic Clinical Trial Liaison with a passion for fostering exceptional site relationships and driving clinical trial success? We're supporting a leading biotech company as they expand their Clinical Operations team in preparation for a pivotal Phase 3 launch later this year. Are you dedicated to providing unparalleled support to investigative sites and thrive in a fast-paced evolving en
job summary: Clinical Trial Liaison | 12 Month Engagement Are you a dynamic Clinical Trial Liaison with a passion for fostering exceptional site relationships and driving clinical trial success? We're supporting a leading biotech company as they expand their Clinical Operations team in preparation for a pivotal Phase 3 launch later this year. Are you dedicated to providing unparalleled support to investigative sites and thrive in a fast-paced evolving en
job summary: A research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: Worcester, Massachusetts job type: Contract salary: $35 - 40 per hour work hour
job summary: A research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: Worcester, Massachusetts job type: Contract salary: $35 - 40 per hour work hour
job summary: A research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: $
job summary: A research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: $
