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Would you like to work in a fast pace and multicultural environment? Then Clariness is the right place to be! Due to our rapid growth, we are looking to recruit a dynamic, service focused Bilingual Junior Site and Patient Relationship Manager.2/10/2015 Piscataway, NJ 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 trial1/24/2015 Cambridge, MA Save This Job
DEPARTMENTClinical Operations and Project Management REPORTS TOSenior Director Clinical Operations and Project Management About Loxo Oncology: Loxo Oncology develops targeted small molecule therapeutics for the treatment of cancer in genetically defined patient populations.12/23/2014 Stamford, CT Save This Job
Verastem is seeking a Clinical Trial Manager to be responsible for high quality and timely execution of clinical trials. Responsibilities Lead study team activities, coordinating internal and external resources along with CRO activities, from study startup through closeout. Work2/26/2015 Needham, MA Save This Job
Department: Clinical Development Job Title: Sr. Manager, Statistical Programming Job Location: San Diego, CA Description: The Statistical Programmer provides statistical programming technical leadership and support to team members including programming outputs (datasets,2/2/2015 San Diego, CA Save This Job
DEPARTMENTClinical Operations and Project Management REPORTS TOClinical Trial Manager About Loxo Oncology: Loxo Oncology develops targeted small molecule therapeutics for the treatment of cancer in genetically defined patient populations. Loxo?s development approach translates12/23/2014 Stamford, CT 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--- protein1/27/2015 Cambridge, 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 class1/13/2015 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 in1/13/2015 Audubon, PA Save This Job
Position Summary: The Clinical Data Coordinator (CDC) serves as CRF Health?s champion to the world?s largest pharmaceutical and biotech companies in providing clean and accurate data for clinical trials. A CDC is the gatekeeper for this data from study start to finish and is core2/16/2015 Plymouth Meeting, PA Save This Job
Program Manager 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 the1/27/2015 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,1/3/2015 Lexington, MA Save This Job
Department(s): Clinical and Regulatory Affairs Reports to: Chief Scientific Officer Company Prolacta is the pioneer in human milk-based nutritional products for premature infants in the neonatal intensive care unit (NICU). Prolacta believes that there is no adequate replacement2/18/2015 City of Industry, CA Save This Job
The Senior Project Manager is responsible for delivering the highest quality clinical trial data capture software & service with on-time delivery. The Senior Project Manager interfaces with clients as well as project teams. In addition, the Senior Project Manager provides1/25/2015 Boston, MA Save This Job
Job Code: 15-635 Location: Rockville, Maryland Applicants must meet the following requirements: Bachelor's Degree required Minimum 3 years of relevant experience in contracting, outsourcing or finance in the clinical trial space The selected candidate will be responsible2/25/2015 Rockville, MD 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 Experienced1/26/2015 Rockville, MD Save This Job
Job Code: 15-485 Location: Rockville, Maryland Applicants must meet the following requirements: Bachelor?s or Master?s degree in the life sciences preferred, plus relevant work experience required. Minimum of 7 years pharmaceutical/biotech research experience with at least 32/25/2015 Rockville, MD 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 systems1/12/2015 Cambridge, MA 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 sites11/17/2014 Marlborough, MA Save This Job
The Project Manager is responsible for delivering the highest quality ePRO software and service with on-time delivery. The Project Manager will interface with clients as well as the project team. Position Responsibilities: Project Management Facilitate gathering requirements1/25/2015 Boston, MA Save This Job