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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 PET8/17/2014 Philadelphia, PA Save This Job
About Acceleron: Acceleron is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel protein therapeutics for cancer and rare diseases. The company is a leader in understanding the biology of the TGF-? protein7/28/2014 Cambridge, MA Save This Job
BIND Therapeutics is hiring a Clinical Trial Manager to join our growing dynamic team. Reporting to the Director of Clinical Operations, the successful candidate will be responsible for all aspects of clinical trial management including but not limited to study planning and8/5/2014 Cambridge, MA Save This Job
Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of underlying cancer biology through its systems8/20/2014 Cambridge, MA 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 Job Location: San Francisco, CA KaloBios is a biopharmaceutical company dedicated to improving the lives of patients with innovative therapies. Our mission is to advance medical care using Humaneered, monoclonal antibodies. KaloBios' Humaneered antibodies8/4/2014 San Francisco, CA 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
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 and8/4/2014 San Francisco, CA Save This Job
Verastem is seeking a motivated and experienced Clinical Trial Supply Manager/Senior Manager to manage all aspects of supplies for clinical studies, including investigational medicinal product and PK/PD kits. The ideal candidate will have strong analytical, organizational,7/29/2014 Cambridge, MA Save This Job
Principal Accountant/Manager, R&D Finance About Acceleron: Acceleron is a publicly traded, clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel protein therapeutics for cancer and rare diseases. The company is a leader8/27/2014 Cambridge, MA Save This Job
Senior Product Manager This Senior Product Manager (SPM) will be responsible for managing the next generation of our data portal software. You will lead cross-functional efforts to solve internal and external Client needs. You will lead and manage a fast paced product8/26/2014 Boston, MA Save This Job
Regulatory Affairs Project Manager Location:Audubon, PA Job Code:RAPMCK0314 Description The Regulatory Affairs Project Manager assists in writing, submitting and gaining approval of 510(k) and IDE/PMA submissions to the Food and Drug administration (FDA) for class II and class7/20/2014 Audubon, PA Save This Job
Merrimack Pharmaceuticals is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack currently has six targeted oncology therapeutics in clinical development.8/20/2014 Cambridge, MA Save This Job
Job Code: 14-403 Location: Rockville, MD Applicants must meet the following requirements: Ph.D. or M.S. in biostatistics or related field with a minimum of 7 years experience in the pharmaceutical, biotechnology, CRO industry or related clinical trials environment Experienced7/28/2014 Rockville, MD Save This Job
SUMMARY: The position reports to the Head of Drug Safety and Pharmacovigilance. The Drug Safety and Pharmacovigilance Operations Manager is independently responsible for the development, management and maintenance of Relypsa?s drug safety and pharmacovigilance program. This8/16/2014 Redwood City, CA Save This Job
Merrimack Pharmaceuticals is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of serious diseases, with an initial focus on cancer. Merrimack currently has six targeted8/20/2014 Cambridge, MA Save This Job
EGeen International Corporation ( www.egeeninc.com ) Location: Sweden or other European countries Posted on: 11:50 AM, September 01, 2008 Position type: Full time Job Code: QA Manager Required education: Bachelor's Degree Area(s) of expertise desired: Quality7/26/2014 Mountain View, CA 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 the8/17/2014 Philadelphia, PA Save This Job
Reports to: Director, Associate Director, or Manager Client Services Department: Client Services Position Summary: The Program Manager is responsible for the timely, high quality delivery of software, hardware and services to PHT?s pharmaceutical clients and the8/26/2014 Boston, 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,8/11/2014 Lexington, MA Save This Job