- 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 oncojob 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, osjob 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: 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 clinicaljob 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 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 busjob 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: 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 locjob 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,
