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Assoc. Director, Clinical Operations? Help Please fill in the information below and use the navigational buttons to continue. Warning: Using your browser's Back and Forward buttons may produce undesirable results. Associate Director, Clinical Operations About Acceleron:8/9/2016 Cambridge, MA Save This Job
Job Description: Works closely with the Clinical Development team for the oversight and execution of assigned clinical studies ?May be responsible for one or more concurrent clinical studies ?Contribute in the development of the clinical study design and writing of the study8/21/2016 Lexington, MA Save This Job
Department: Clinical Operations Job Title: Associate Director, Clinical Program Manager Reports To: Senior Director, Clinical Operations Description: Lead the development and execution of operational strategies for multiple molecules/programs in the company?s8/24/2016 Philadelphia, PA Save This Job
Location: Stamford, CT Reports To: Associate Director Clinical Operations Position Description: Functions as the clinical study team leader to plan, organize, and coordinate all operational aspects of a clinical study from protocol development through database lock. Ensures9/7/2016 Stamford, CT Save This Job
June 10, 2016 Job description We are searching for a talented Clinical Operations expert who is willing to build the Clinical Operations function at Sound Pharmaceuticals from the ground up. The Director of Clinical Operations will be accountable for the operational strategic8/1/2016 Seattle, WA Save This Job
Position Summary The Director, Clinical Quality Operations will work directly with Clinical Development to assure that all aspects of Clinical Operations are in compliance with GCP, corporate and departmental policies and procedures, and all applicable worldwide regulations.8/14/2016 San Francisco, CA Save This Job
The Director/Assoc. Director of Clinical Supply Chain ensures that all clinical trials have timely and adequate supply for administration to subjects. The Clinical Supply Chain group is involved in a clinical trial from the early stages of inception to study closure. This role9/13/2016 San Francisco, CA Save This Job
Position Summary: The Director, Clinical Quality Compliance will play a key role in managing FibroGen?s Clinical QA audit program. The individual?s focus will be on managing and conducting internal and external audits to assure that clinical trials are conducted in8/14/2016 San Francisco, CA Save This Job
The Associate Director/Director, Regulatory Operations reports to the VP Regulatory Affairs. This position is responsible for the oversight and management of day-to-day Regulatory submissions to Global Health Authorities (i.e., FDA, Health Canada, EMEA, SFDA, etc.). This8/14/2016 San Francisco, CA Save This Job
TARIS Biomedical is a unique therapeutically-focused urology company developing drug-device combination products for the treatment of genitourinary diseases. The Associate Director of Clinical Quality Assurance will provide leadership and expertise to support TARIS? pipeline8/27/2016 Lexington, MA Save This Job
Clinical/ Laboratory Cambridge, Massachusetts Apply Good Start Genetics is a molecular genetics information company transforming the standard of care in reproductive medicine. Its suite of reproductive genetics products provides clinicians and patients with insightful and8/7/2016 Cambridge, MA Save This Job
Clinical/ Laboratory Cambridge, MA, United States Good Start Genetics is a molecular genetics information company transforming the standard of care in reproductive medicine. Its suite of reproductive genetics products provides clinicians and patients with insightful and8/7/2016 Cambridge, MA Save This Job
The Director, Program Management (level to be determined based on experience) is responsible to ensure adherence to the project scope, timeline and budget, and intervenes when necessary to identify and resolve issues in order to ensure timely completion of the drug development9/13/2016 San Francisco, CA Save This Job
June 10, 2016 Reports to: Sr. Director Clinical or designee Status: Exempt Job description The role of the Senior Clinical Research Associate (CRA) is to support several ongoing and upcoming clinical trials (Phase 1b through Phase 3).8/1/2016 Seattle, WA Save This Job
Reports to: Vice President, Clinical Development Education: Board certification in Internal Medicine, and preferably additional Board Certification in Pulmonary Medicine or Oncology Job Description This role represents a unique opportunity for a physician experienced in8/1/2016 Boston, MA Save This Job
Job Summary: Working within the clinical development organization, the Scientist will support multiple programs, performing PK analyses for Phase 1 studies and provide input to the development of clinical study designs and protocols. A strong background in pharmacokinetics8/21/2016 Lexington, MA Save This Job
Summary The Clinical Workflow Architect (CWA) is responsible for working with MD Revolution?s clients to ensure that recommended workflows are successfully deployed, implemented, and adopted. This person is the ?change agent? for MDR, making sure that the client successfully8/13/2016 San Diego, CA Save This Job
Cambridge, Massachusetts Job description PatientsLikeMe (PLM) has an immediate opening for a Manager (or Director, depending on experience) to help create the next generation of services we offer our client partners. Sitting within the Commercial Offerings team in the PLM9/5/2016 Cambridge, MA Save This Job
Department: Regulatory Affairs Position Type / FLSA Status: Full Time / Exempt Location: Emeryville, CA Position Summary This position is primarily responsible for developing, coordinating and implementing regulatory strategies for new product development registrations,8/1/2016 Emeryville, CA Save This Job
Job Code: 2016-70-2 Job Summary The Senior Director, Medical Oncology will be a critical member of the Clinical Development team and contribute to the Company?s drug development programs. The Senior Director, Medical Oncology will perform various duties in support of clinical8/9/2016 Gaithersburg, MD Save This Job