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Verastem is seeking a Clinical Trial Manager to be responsible for assisting Study Leads with the day-to-day management of contract CROs conducting Verastem sponsored clinical trials, as well as various other clinical trial management tasks. Responsibilities Work with CROs to10/1/2014 Cambridge, MA Save This Job
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 leader in understanding the biology of the TGF-?9/30/2014 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 PET8/17/2014 Philadelphia, PA 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 trial8/26/2014 Cambridge, MA 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,10/1/2014 Cambridge, MA 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,9/1/2014 Cambridge, MA Save This Job
Description: The Associate Manager/Sr. Manager, Clinical Contracts will play an integral role in the execution of the Company?s clinical studies. The successful incumbent will be primarily responsible for vendor contracts in the Fibrosis programs. However, this role could8/4/2014 San Francisco, CA 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
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 the9/1/2014 Cambridge, MA 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-? protein9/30/2014 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 the8/17/2014 Philadelphia, PA 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 class8/23/2014 Audubon, PA Save This Job
Description Clinical Data Monitor The position is responsible for performing monitoring activities associated with all ongoing Class III FDA-related clinical studies. This individual will need to perform site monitoring visits by adhering to the schedule established in8/23/2014 Audubon, PA 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
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 Experienced8/31/2014 Rockville, MD Save This Job
ID 2014-1242 # of Openings 1 Department Clinical Affairs Posted Date 9/29/2014 Job Location US-MA-Marlborough More information about this job: Overview: In-house professional responsible for supporting the initiation, monitoring, and closing out of clinical study sites10/1/2014 Marlborough, MA Save This Job
Reports to: Senior Director, ProCURE Business Segment Status: Full-time Please combine your cover letter and resume in one Word or PDF file, only one document may be uploaded through the online application process. Emailed resumes will not be accepted. Stemgent-Asterand9/3/2014 Detroit, MI 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
Requisition Number: PM0010 ApoCell is a molecular diagnostic testing company located near the Houston Medical Center. ApoCell has proprietary core technology used to facilitate the development of drugs in clinical trials and predict patient response to therapy. We are searching8/13/2014 Houston, TX 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: Quality8/26/2014 Mountain View, CA Save This Job