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The Senior Director, Clinical Research will have hands-on responsibility designing clinical trials focused on assigned therapeutic areas and will exhibit a passion for Phases 1 through 3, including biomarkers, proof-of-concept and full developmenty. Responsibilities Design and7/29/2014 Cambridge, MA Save This Job
Department: Clinical Operations Job Title: Clinical Research Associate II Reports To: Senior Director, Clinical Operations Description: Position Overview: The Clinical Research Associate II provides administrative and technical support related to clinical trials to the7/13/2014 Philadelphia, PA Save This Job
Job Details Level: ExperiencedSalary Range: Undisclosed Job Location: USA-AZ-ScottsdaleTravel %: Up to 50% Position Type: Full TimeJob Shift: Day Education Level: 4 Year DegreeJob Category: Research Description The Director of Clinical Research (DCR) is responsible for the7/6/2014 Scottsdale, AZ Save This Job
Description The Project Manager, Clinical Research will be responsible for conducting post marketing clinical research on Globus Medical products. The candidate should have demonstrated abilities to conduct clinical trials and work with product development, marketing, surgeons,7/20/2014 Audubon, PA Save This Job
Company Overview: Cerecor Inc ("Cerecor" or the "Company") is a biopharmaceutical company focused on the discovery, development and commercialization of prescription pharmaceuticals whose primary activity is in the human brain. Position Summary: The individual will be part of8/2/2014 Baltimore, MD Save This Job
We are seeking a Manager of Clinical Research to join the Clinical Operations team at Catabasis. The role will be a key contributor to the company?s clinical development and primarily responsible for the hands-on management and monitoring of clinical studies in the7/29/2014 Cambridge, MA Save This Job
We are seeking a Senior Clinical Research Associate to join the Clinical Operations team at Catabasis. The role will be a key contributor to the company?s clinical development and primarily responsible for the hands-on management and monitoring of clinical studies in7/29/2014 Cambridge, MA Save This Job
Brief Position Summary: FORUM Pharmaceuticals is seeking a Medical Director/Senior Director of Clinical Research with psychiatry experience to join the FORUM Clinical Research Team. He/She will have the opportunity to work on a compound in late-stage development providing8/11/2014 Watertown, MA Save This Job
Description: Join a growing Clinical team dedicated to support FibroGen?s first in class global anemia program consisting of three global Phase 3 studies. Located on a beautiful waterfront property in San Francisco, FibroGen is seeking Clinical Research Professionals who have a6/30/2014 San Francisco, CA Save This Job
Description: Located in San Francisco, FibroGen seeks a highly qualified Sr. CRA or CTM to join a dynamic team devoted to a Phase I, study for subjects with locally advanced or metastatic pancreatic cancer. This is a US based trial partially monitored by a CRO, but offers the6/30/2014 San Francisco, CA Save This Job
Department: Clinical Research Services Reports to: Senior Director, Global Head of Biostatistics Locations: 1. Waltham, MA, 2. Chesterbrook, PA Company Profile Cytel Inc. is a leading provider of clinical research services and trial design and analysis software/services6/30/2014 Waltham, MA Save This Job
SUMMARY: The Senior/Executive Director of Biostatistics oversees the Biostatistics Department within Relypsa and functions as a Senior Biostatistician on projects as needed. The Biostatistics Department is responsible for the statistical aspects of clinical trials, including8/12/2014 Redwood City, CA Save This Job
SUMMARY: The Director of Biostatistics is responsible for the statistical aspects of all clinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting8/12/2014 Redwood City, CA Save This Job
SUMMARY: The Director of Biostatistics is responsible for the statistical aspects of all clinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting7/13/2014 Redwood City, CA Save This Job
Job Summary Assists Director or Project Management in leading teams and conducting programs including tracking and reporting study progress, metrics, continuity, compliance, budget and quality of clinical trials. Responsible for creating and maintaining regulatory adherent trial8/25/2014 Cambridge, MA Save This Job
Department: Clinical Operations Job Title: Clinical Data Manager Reports To: Senior Director, Clinical Operations Description: Avid Radiopharmaceuticals, Inc. (Avid RP), a wholly owned subsidiary of Eli Lilly and Company, is a molecular imaging company developing novel PET7/13/2014 Philadelphia, PA Save This Job
Description: FibroGen seeks a Clinical Quality Assurance (CQA) Associate Director / Senior Manager to support the company?s Clinical Quality Assurance program. The incumbent will conduct and manage Good Clinical Practice (GCP) related quality audits (e.g., investigator site and6/30/2014 San Francisco, CA Save This Job
SUMMARY: Relypsa is a clinical-stage biopharmaceutical company focused on the development and commercialization of non-absorbed polymeric drugs to treat disorders in the areas of renal, cardiovascular and metabolic diseases. The Director of Biology / Pharmacology will play a7/13/2014 Redwood City, CA Save This Job
Job Description PatientsLikeMe is looking for a talented and proven Program Director to lead key customer relationships. Someone who is data-driven and analytical at heart. Someone who is willing to roll up their sleeves and get deep into our data with customers. Someone who7/27/2014 Cambridge, MA Save This Job
Job Summary: Works closely with VP, Clinical Operations for the oversight and execution of assigned clinical studies Responsibilities: Contribute in the development/writing of Clinical Protocol Contribute in the review of all study related documentation (Clinical Protocol,7/7/2014 Lexington, MA Save This Job