job summary: Job Description As we expand our business, we seek a motivated and skilled API Programming Intern to join our team and help develop advanced APIs that power our products and services location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors responsibilities: Job Responsibilities Support EDC User Management and Site Administration activities.Understand how to build RESTful AP
job summary: Job Description As we expand our business, we seek a motivated and skilled API Programming Intern to join our team and help develop advanced APIs that power our products and services location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors responsibilities: Job Responsibilities Support EDC User Management and Site Administration activities.Understand how to build RESTful AP
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: Job Description The Medical Writing Intern (MWI) assists with medical writing activities in support of the GCDO - Medical Writing & Transparency department. The MWI works closely with MW personnel to develop regulatory documents in support of company products. This individual will work to assigned timelines, communicate effectively to the responsible medical writer, and ensure their deliverables are completed according to appropriate quality
job summary: Job Description The Medical Writing Intern (MWI) assists with medical writing activities in support of the GCDO - Medical Writing & Transparency department. The MWI works closely with MW personnel to develop regulatory documents in support of company products. This individual will work to assigned timelines, communicate effectively to the responsible medical writer, and ensure their deliverables are completed according to appropriate quality
job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco
job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco
job summary: About the Company A global Pharmaceutical company that harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, os
job summary: About the Company A global Pharmaceutical company that harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, os
job summary: The Sr. Clinical Trial Manager (CTM) is responsible for the overall management and oversight of assigned clinical trials and clinical research. The Sr. CTM will be a key contributor to develop study-related documents and create standards and guidelines for clinical research studies and programs ensuring adherence to standard operating procedures, International Conference on Harmonisation/ Good Clinical Practice (ICH-GCP), and FDA regulations.
job summary: The Sr. Clinical Trial Manager (CTM) is responsible for the overall management and oversight of assigned clinical trials and clinical research. The Sr. CTM will be a key contributor to develop study-related documents and create standards and guidelines for clinical research studies and programs ensuring adherence to standard operating procedures, International Conference on Harmonisation/ Good Clinical Practice (ICH-GCP), and FDA regulations.
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: 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
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: 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: 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: 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: 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 Regulatory Operations Publishing | Undergrad Intern ~ Summer 2024 Are you a detail-oriented student eager to gain hands-on experience in Regulatory Operations and global health authority submissions? This internship offers a unique opportunity to contribute to the preparation and delivery of high-quality, timely, and compliant regulatory submissions in a fast-paced, cross-functional environment. As a Global Regulatory Publishing Under
job summary: Global Regulatory Operations Publishing | Undergrad Intern ~ Summer 2024 Are you a detail-oriented student eager to gain hands-on experience in Regulatory Operations and global health authority submissions? This internship offers a unique opportunity to contribute to the preparation and delivery of high-quality, timely, and compliant regulatory submissions in a fast-paced, cross-functional environment. As a Global Regulatory Publishing Under
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: Immediate opportunity for an experienced, Specialist Product Quality, to manage change control, deviations, and compliance records for biologics and synthetic chemical manufacturing. The Specialist Product Quality will collaborate cross-functionally with Supply Chain, Manufacturing, Quality Control, Regulatory, and other teams to ensure quality and compliance. Key Responsibilities include: Own and review change control, deviation records, a
job summary: Immediate opportunity for an experienced, Specialist Product Quality, to manage change control, deviations, and compliance records for biologics and synthetic chemical manufacturing. The Specialist Product Quality will collaborate cross-functionally with Supply Chain, Manufacturing, Quality Control, Regulatory, and other teams to ensure quality and compliance. Key Responsibilities include: Own and review change control, deviation records, a
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: A current top partnership with 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 impact 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 current top partnership with 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 impact 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: $
