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 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: Real-World Evidence & Biostatistics ~ Exclusive Summer Internship Opportunity We're looking for a highly motivated Master's or PhD student to join our Real-World Evidence (RWE) and Biostatistics research team for a Summer Internship. This role will focus on the application of Double Machine Learning in Causal Inference, providing exposure to real-world healthcare data and advanced statistical modeling techniques. The intern will work with cr
job summary: Real-World Evidence & Biostatistics ~ Exclusive Summer Internship Opportunity We're looking for a highly motivated Master's or PhD student to join our Real-World Evidence (RWE) and Biostatistics research team for a Summer Internship. This role will focus on the application of Double Machine Learning in Causal Inference, providing exposure to real-world healthcare data and advanced statistical modeling techniques. The intern will work with cr
job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight
job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight
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: The MedComm Writer will be accountable for drafting and reviewing scientifically accurate, original content for medical and promotional Pharmaceutical clients. In this role you will work with clients and the Scientific Strategy Lead to plan and develop high-impact, innovative medical communications for assigned brands. You will play a significant role in account growth by building trust with clients through scientific exchange and expertise i
job summary: The MedComm Writer will be accountable for drafting and reviewing scientifically accurate, original content for medical and promotional Pharmaceutical clients. In this role you will work with clients and the Scientific Strategy Lead to plan and develop high-impact, innovative medical communications for assigned brands. You will play a significant role in account growth by building trust with clients through scientific exchange and expertise i
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: 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 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: Project Manager - Clinical Trial Process Optimization Exciting opportunity to drive innovation in clinical trial processes! 4 Openings: (3) Traditional PMs (1) Change Management PM Salaried Contract - 12 Months w/Full Benefits | Remote Join a high-impact team within a large pharmaceutical company, supporting continuous improvement and change management initiatives across the end-to-end clinical trial process. This role offers visibility and
job summary: Project Manager - Clinical Trial Process Optimization Exciting opportunity to drive innovation in clinical trial processes! 4 Openings: (3) Traditional PMs (1) Change Management PM Salaried Contract - 12 Months w/Full Benefits | Remote Join a high-impact team within a large pharmaceutical company, supporting continuous improvement and change management initiatives across the end-to-end clinical trial process. This role offers visibility and
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: 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: 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: $
job summary: Biostatistics Intern ~ Summer 2024 Are you a PhD student in Statistics, Biostatistics, Data Science, or Mathematics looking to gain hands-on experience in the pharmaceutical industry? Our 10-week Data Science Internship Program offers an exciting opportunity to apply your statistical expertise to real-world drug development challenges. As a Biostatistics Intern, you will: Gain a deeper understanding of the drug development process and stati
job summary: Biostatistics Intern ~ Summer 2024 Are you a PhD student in Statistics, Biostatistics, Data Science, or Mathematics looking to gain hands-on experience in the pharmaceutical industry? Our 10-week Data Science Internship Program offers an exciting opportunity to apply your statistical expertise to real-world drug development challenges. As a Biostatistics Intern, you will: Gain a deeper understanding of the drug development process and stati
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: 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: 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: 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: We are seeking an experienced medical writing leader in medical communications to join an award-winning in-house agency at a major pharmaceutical company. This remote position offers the opportunity to work with a small but growing team in a long-term, salaried contract role. location: Telecommute job type: Outsourcing Project salary: $87 - 94 per hour work hours: 9 to 5 education: Doctorate responsibilities: Lead a team o
job summary: We are seeking an experienced medical writing leader in medical communications to join an award-winning in-house agency at a major pharmaceutical company. This remote position offers the opportunity to work with a small but growing team in a long-term, salaried contract role. location: Telecommute job type: Outsourcing Project salary: $87 - 94 per hour work hours: 9 to 5 education: Doctorate responsibilities: Lead a team o
job summary: We are seeking a Regulatory Submission Manager to support global regulatory initiatives and ensure compliance with regulatory requirements for investigational and marketed products. Role involves working closely with cross-functional teams and regulatory leads to support submission activities, labeling development, and strategic regulatory guidance. The ideal candidate has a strong background in regulatory submissions and document review, as
job summary: We are seeking a Regulatory Submission Manager to support global regulatory initiatives and ensure compliance with regulatory requirements for investigational and marketed products. Role involves working closely with cross-functional teams and regulatory leads to support submission activities, labeling development, and strategic regulatory guidance. The ideal candidate has a strong background in regulatory submissions and document review, as
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: 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: We are seeking an experienced Regulatory Writer with a strong background in writing protocols, clinical study reports (CSRs), briefing books, informed consent forms (ICFs), and CTD Module 2 documents. This expertise is critical to the role. The successful candidate will play a key role in preparing high-quality regulatory documentation to support clinical and regulatory submissions, ensuring compliance with global regulatory requirements. Thi
job summary: We are seeking an experienced Regulatory Writer with a strong background in writing protocols, clinical study reports (CSRs), briefing books, informed consent forms (ICFs), and CTD Module 2 documents. This expertise is critical to the role. The successful candidate will play a key role in preparing high-quality regulatory documentation to support clinical and regulatory submissions, ensuring compliance with global regulatory requirements. Thi
