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Clinical Study Manager Jobs

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Clinical Trial Manager II

GlycoMimetics

Clinical Research Associate II Reports to: Clinical Trial Manager II Job Code: 2015-70-3 Job Summary The Clinical Research Associate II (CRA II) will provide in-house support for clinical trial operations including management of clinical trial sites and Contract Research

3/2/2015  Gaithersburg, MD  Save This Job

Clinical Trial Manager (15-102)

FibroGen

Job Location: San Francisco, CA Description: FibroGen seeks a highly motivated Senior Clinical Research Associate (Sr. CRA). This position focuses on Global Phase 3 study execution for the FibroGen anemia program and may also have responsibility for specific tasks including

3/4/2015  San Francisco, CA  Save This Job

Senior Clinical Trial Manager/Clinical Trial Manager

Verastem

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. Work

2/26/2015  Needham, MA  Save This Job

Clinical Trial Manager

Merrimack Pharmaceuticals

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 systems

1/12/2015  Cambridge, MA  Save This Job

Clinical Trial Manager

Merrimack Pharmaceuticals

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 systems

1/12/2015  Cambridge, MA  Save This Job

Clinical Project Manager

Genocea Biosciences, Inc.

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 trial

1/24/2015  Cambridge, MA  Save This Job

Clinical Project Manager (15-639)

MacroGenics

Job Code: 15-639 Location: Rockville, Maryland Applicants must meet the following requirements: Bachelor's Degree or higher; science background desirable Minimum 3 years experience in clinical project management Oncology clinical trial experience required Approximately 20%

2/25/2015  Rockville, MD  Save This Job

Clinical Project Manager (14-517)

MacroGenics

Job Code: 14-517 Location: South San Francisco, CA Applicants must meet the following requirements: Bachelor degree or higher, science background desirable Minimum of 3 years experience in clinical project management Oncology clinical trial experience required Approximately

2/25/2015  South San Francisco, CA  Save This Job

Clinical Trial Associate (14-932)

MacroGenics

Job Code: 14-932 Location: South San Francisco, CA Applicants must meet the following requirements: Bachelor?s Degree or relevant experience Minimum of 2 ? 5 years of administrative experience; clinical experience preferred Demonstrated proficiency with Microsoft Office,

2/25/2015  South San Francisco, CA  Save This Job

Clinical Trial Associate (15-640)

MacroGenics

Job Code: 15-640 Location: Rockville, Maryland Applicants must meet the following requirements: Bachelor?s Degree or relevant experience Minimum of 2 ? 5 years of administrative experience; clinical experience preferred Demonstrated proficiency with Microsoft Office,

2/25/2015  Rockville, MD  Save This Job

Manager, Statistical Programming (15-103)

FibroGen

Job Location: San Francisco, CA Description: Responsible for management statistical programming activities and study related projects while also developing and implementing SAS programs to efficiently produce analyses. Exercise judgment within generally defined practices and

3/4/2015  San Francisco, CA  Save This Job

Regulatory Affairs Project Manager

Globus Medical

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 class

1/13/2015  Audubon, PA  Save This Job

Sr. Manager, Quality Assurance Auditor

Ambit Biosciences

Department: Regulatory Affairs Job Title: Sr. Manager, Quality Assurance Auditor Job Location: San Diego, CA Description: The Q.A. Auditor will work with the Quality Assurance team to develop and fulfill an efficient and effective plan to maximize the value of Ambit?s

2/2/2015  San Diego, CA  Save This Job

Sr. Clinical Research Associate

Oxford Immunotec

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 sites

11/17/2014  Marlborough, MA  Save This Job

Sr. Biostatistician/Manager (14-403)

MacroGenics

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 Experienced

1/26/2015  Rockville, MD  Save This Job

National Account Manager

Merrimack Pharmaceuticals

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 targeted

1/12/2015  Cambridge, MA  Save This Job

Manager, Clinical Research

Prolacta Bioscience

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 replacement

2/18/2015  City of Industry, CA  Save This Job

Study Design Analyst

PHT

The Study Design Analyst (Design Services) is responsible for delivering the highest quality ePRO and eCOA systemdesign, specifications development and server as a subject matter expert for PHT clients.. The position will be aligned with one or more project teams, interface with

1/25/2015  Boston, MA  Save This Job

Study Site Orientation Specialist

Acurian

Reports to: Project Start Up Team Lead Acurian is offering an exciting new opportunity for an experienced professional with a strong background in training and sales, (software sales a real plus), and looking for a different challenge within the pharmaceutical industry. Acurian

2/2/2015  Horsham, PA  Save This Job