job summary: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatment
job summary: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatment
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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: Job Summary In this role, you will be responsible for providing quality assurance network support for contract manufacturing and testing. You are responsible for ensuring that all batch-related activities, including receipt, review, and release of Bulk Drug Substance (BDS) and Drug Product (DP), are conducted in compliance with regulatory standards. This role is focused on executing Batch Record Release activities following Drug Product CMO R
job summary: Job Summary In this role, you will be responsible for providing quality assurance network support for contract manufacturing and testing. You are responsible for ensuring that all batch-related activities, including receipt, review, and release of Bulk Drug Substance (BDS) and Drug Product (DP), are conducted in compliance with regulatory standards. This role is focused on executing Batch Record Release activities following Drug Product CMO R
job summary: Job Summary In this role, you will be responsible for providing quality assurance network support for contract manufacturing and testing. You are responsible for ensuring that all batch-related activities, including receipt, review, and release of Bulk Drug Substance (BDS) and Drug Product (DP), are conducted in compliance with regulatory standards. This role is focused on executing Batch Record Release activities following Drug Product CMO R
job summary: Job Summary In this role, you will be responsible for providing quality assurance network support for contract manufacturing and testing. You are responsible for ensuring that all batch-related activities, including receipt, review, and release of Bulk Drug Substance (BDS) and Drug Product (DP), are conducted in compliance with regulatory standards. This role is focused on executing Batch Record Release activities following Drug Product CMO R
job summary: Ensures accurate and consistent coding of medical data, including but not limited to, adverse event verbatim descriptions and medication data received from global clinical trials across all clinical areas including identification of prohibited medications and exclusionary medical history. Participates in Centralized Clinical Coding Group (CCCG) process improvement initiatives and serves as a subject matter expert and primary coding resource f
job summary: Ensures accurate and consistent coding of medical data, including but not limited to, adverse event verbatim descriptions and medication data received from global clinical trials across all clinical areas including identification of prohibited medications and exclusionary medical history. Participates in Centralized Clinical Coding Group (CCCG) process improvement initiatives and serves as a subject matter expert and primary coding resource f
job summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meet
job summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meet
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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
job summary: This is a high level contract role, requiring Direct Global Regulatory Labeling Operations Project Management experience in the Pharma/Biotech industry, as deep knowledge of pharmaceutical labeling regulations, compliance, and processes are critical for this role. The Labeling Project Manager is responsible for all activities associated with the development, creation and execution of labeling for assigned product lines for domestic and/or i
job summary: This is a high level contract role, requiring Direct Global Regulatory Labeling Operations Project Management experience in the Pharma/Biotech industry, as deep knowledge of pharmaceutical labeling regulations, compliance, and processes are critical for this role. The Labeling Project Manager is responsible for all activities associated with the development, creation and execution of labeling for assigned product lines for domestic and/or i
job summary: The Global Regulatory Operations Publishing Intern prepares and delivers high quality, timely, and compliant regulatory submissions to global health authorities. The Publishing Intern represents Global Regulatory Publishing in cross-functional project teams, provides regulatory submission support for products and contributes to regulatory initiatives location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9
job summary: The Global Regulatory Operations Publishing Intern prepares and delivers high quality, timely, and compliant regulatory submissions to global health authorities. The Publishing Intern represents Global Regulatory Publishing in cross-functional project teams, provides regulatory submission support for products and contributes to regulatory initiatives location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9
job summary: Required: Must be currently enrolled in a Bachelor's degree program (Junior/Senior level)No industry experience requiredStrong verbal and written communication skillsBasic knowledge of Word, Excel, PowerPoint, and shared platforms (e.g., SharePoint, Box, Smartsheets) Preferred: Exposure to Good Clinical Practices (GCP) regulations and Standard Operating Procedures (SOPs)Understanding of clinical study phases and their role in clinical
job summary: Required: Must be currently enrolled in a Bachelor's degree program (Junior/Senior level)No industry experience requiredStrong verbal and written communication skillsBasic knowledge of Word, Excel, PowerPoint, and shared platforms (e.g., SharePoint, Box, Smartsheets) Preferred: Exposure to Good Clinical Practices (GCP) regulations and Standard Operating Procedures (SOPs)Understanding of clinical study phases and their role in clinical
job summary: As the world's 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. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare
job summary: As the world's 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. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare
job summary: Our client is seeking a Senior or Principal Statistician to support Synthetic Control Arm (SCA) projects in late-phase oncology trials, with a primary focus on SAS, CDISC, and ADaM. This is a fully remote, 6-month contract (potential to extend). location: New York, New York job type: Contract salary: $110 - 120 per hour work hours: 9 to 5 education: Doctorate responsibilities: Primarily support late-phase oncology trials (
job summary: Our client is seeking a Senior or Principal Statistician to support Synthetic Control Arm (SCA) projects in late-phase oncology trials, with a primary focus on SAS, CDISC, and ADaM. This is a fully remote, 6-month contract (potential to extend). location: New York, New York job type: Contract salary: $110 - 120 per hour work hours: 9 to 5 education: Doctorate responsibilities: Primarily support late-phase oncology trials (
job summary: We are seeking a Clinical Site Contracts Specialist to manage end-to-end processes for clinical site contracts and consulting agreements, ensuring smooth study start-up and trial operations. If you're detail-oriented, proactive, and passionate about negotiation and collaboration, this is your chance to contribute to critical clinical research initiatives. Apply today to take the next step in your career-let's start the conversation! locati
job summary: We are seeking a Clinical Site Contracts Specialist to manage end-to-end processes for clinical site contracts and consulting agreements, ensuring smooth study start-up and trial operations. If you're detail-oriented, proactive, and passionate about negotiation and collaboration, this is your chance to contribute to critical clinical research initiatives. Apply today to take the next step in your career-let's start the conversation! locati
job summary: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours | RATE (TBD awaiting confirmation) Join a mission-driven team committed to ensuring the safe and effective use of pharmaceutical products worldwide. We're seeking a Global Labeling Manager with a passion for regulatory excellence, precision, and cross-functional collaboration. About the Role: As a Global Labeling Manager, you will drive global labeling strategy and ensure high-qu
job summary: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours | RATE (TBD awaiting confirmation) Join a mission-driven team committed to ensuring the safe and effective use of pharmaceutical products worldwide. We're seeking a Global Labeling Manager with a passion for regulatory excellence, precision, and cross-functional collaboration. About the Role: As a Global Labeling Manager, you will drive global labeling strategy and ensure high-qu
job summary: A precision medicine company using innovative science to improve patient care and solve serious and costly problems. We are working to narrow the gap between scientific innovation and clinical decision- If you're passionate about having an impact on medicine, we'd love to hear from you. location: Telecommute job type: Permanent salary: $130,000 - 140,000 per year work hours: 9 to 5 education: Bachelors responsibilities: This
job summary: A precision medicine company using innovative science to improve patient care and solve serious and costly problems. We are working to narrow the gap between scientific innovation and clinical decision- If you're passionate about having an impact on medicine, we'd love to hear from you. location: Telecommute job type: Permanent salary: $130,000 - 140,000 per year work hours: 9 to 5 education: Bachelors responsibilities: This
job summary: **Must have a PHD** **Must be familiar with mouse models** **Bilingual in Mandarin/English is Preferred** Randstad Life Sciences is working with a fast-growing biotech company with broad cutting-edge technologies. You will have the best opportunity to learn and utilize the science and business in the fields of immunooncology, animal model gene engineering, preclinical pharmacology, therapeutic antibody discovery, etc. The biggest advantage of
job summary: **Must have a PHD** **Must be familiar with mouse models** **Bilingual in Mandarin/English is Preferred** Randstad Life Sciences is working with a fast-growing biotech company with broad cutting-edge technologies. You will have the best opportunity to learn and utilize the science and business in the fields of immunooncology, animal model gene engineering, preclinical pharmacology, therapeutic antibody discovery, etc. The biggest advantage of
job summary: Regulatory Medical Writer - Protocols/Immunology We are seeking an experienced Regulatory Medical Writer to support a small biotech on a part-time contract basis. This role will focus on developing and revising protocols and amendments for three Phase III immunology studies. Contract: Through 12/31/25 Hours: PT~10-20 hours per week Rate: $110-120 per hour w2 only Therapeutic Area: Immunology Focus: Phase III protocols & amendments loc
job summary: Regulatory Medical Writer - Protocols/Immunology We are seeking an experienced Regulatory Medical Writer to support a small biotech on a part-time contract basis. This role will focus on developing and revising protocols and amendments for three Phase III immunology studies. Contract: Through 12/31/25 Hours: PT~10-20 hours per week Rate: $110-120 per hour w2 only Therapeutic Area: Immunology Focus: Phase III protocols & amendments loc
job summary: Job Description Intern, Global Patient and Site Engagement, will be a member of the GPSE team under GCDO. The Intern will work cross functionally across the portfolio supporting the vision to bring the patient and site voice into the clinical design and clinical trial working group teams, as well as study feasibility and global monitoring with activities related to site relationship management, strategic planning for new and ongoing studies,
job summary: Job Description Intern, Global Patient and Site Engagement, will be a member of the GPSE team under GCDO. The Intern will work cross functionally across the portfolio supporting the vision to bring the patient and site voice into the clinical design and clinical trial working group teams, as well as study feasibility and global monitoring with activities related to site relationship management, strategic planning for new and ongoing studies,
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. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowled
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. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowled
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. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowle
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. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowle
job summary: Sr. Medical Editor - Medical Communications REMOTE / Part-Time 20 hrs/wk | EST Hours ELS Certification Required (Editor in the Life Sciences) via Board of Editors in Life Sciences (BELS) Randstad is hiring a Senior Editor for Scientific Services to join an award-winning, best-in-class in-house agency at a leading pharmaceutical company. This full-service agency develops cutting-edge digital, video, AR/VR, and print assets, consistently outper
job summary: Sr. Medical Editor - Medical Communications REMOTE / Part-Time 20 hrs/wk | EST Hours ELS Certification Required (Editor in the Life Sciences) via Board of Editors in Life Sciences (BELS) Randstad is hiring a Senior Editor for Scientific Services to join an award-winning, best-in-class in-house agency at a leading pharmaceutical company. This full-service agency develops cutting-edge digital, video, AR/VR, and print assets, consistently outper
