- Aequor (Raleigh, NC)
- …in Excel and Word will be required during submission. Purpose / Accountabilities Provide clinical site contracting services to clinical study teams to ... activities - Negotiate clinical site contracts (ie Disclosure Agreements, Clinical Trial Agreements, Service Agreements) using appropriate guidelines and… more
- Insmed Incorporated (NJ)
- …related to ongoing and planned trials, management of third-party vendors for clinical services , management of project timelines and deliverables. Key trial ... future of science, we're in. Are you?About the Role:The Clinical Trial Manager will be responsible for the management...management support to the Associate Directors (CST Leads), as assigned.What You'll Do: Leads… more
- Insmed Incorporated (NJ)
- …the future of science, we're in. Are you?About the Role:The Associate Director, Programming provides technical leadership and ensures adequate programming support ... of Programming strategies and efficient execution of analyses for assigned clinical projects. Collaborates with cross-functional team members within Biometrics, … more
- Insmed Incorporated (St. Louis, MO)
- …a local medical and scientific resource to Insmed for product planning, clinical insights, and intelligence. Collect, synthesize and deliver HCP derived scientific ... insights to Insmed.Support research and development programs as requested by R&D, Clinical Operations, and Medical Affairs Departments. This may include trial site… more
- Eisai, Inc (Dallas, TX)
- …difference. If this is your profile, we want to hear from you. The Associate Director, Access and Reimbursement (AD ARM) will lead the Eisai Access and Reimbursement ... reimbursement issues, including Payer Markets, Market Access and Reimbursement Services , Sales, Marketing, Government Affairs, Legal, Compliance, Medical, and… more
- Insmed Incorporated (NJ)
- …future of science, we're in. Are you?About the Role:We're looking for an Associate , Regulatory Operations on the Regulatory team to help us expand what's possible ... and regulatory archives.Partner with cross-functional teams (Regulatory Affairs, CMC, Clinical , Quality) to facilitate document authoring, review, approval, and… more
- Insmed Incorporated (NJ)
- …science, we're in. Are you?About the Role:This is a REMOTE position. The Associate Director of Field Medical Excellence (FME) will implement field medical functional ... high-quality, impactful customer engagements with a consistent approach worldwide. The Associate Director FME will also drive operational excellence across the… more
- Insmed Incorporated (Minneapolis, MN)
- …for the future of science, we're in. Are you?About the Role:The Associate Director Medical Science Liaison will develop and maintain professional relationships with ... a local medical and scientific resource to Insmed for product planning, clinical insights, and intelligence. Bring together, synthesize and deliver HCP derived… more
- Merck & Co. (Rahway, NJ)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post...to have a minimum of twelve (12) months of service in current position prior to applying for open… more
- ACROBiosystems Inc. (San Jose, CA)
- …proteins and critical reagents/assays to support drug development and clinical applications from target discovery and validation, candidate drug screening ... and optimization, CMC development, preclinical and clinical studies, commercial production, and companion diagnostics. We are committed to excellence in providing… more
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