Clinical Trial Manager - Contract - Oncology Phase I (Remote)

Job Type:
Clinical Research
Job Category:
Study Managers
Salary Description:
Competitive Salary
Job Ref:

My client is seeking a Clinical Trial Manager for a 2 – 3 month contract starting ASAP. This is a home based (remote) role offering a competitive hourly rate. If you are seeking a CTM role for a high paid rate then this is a great opportunity, perfect for a contractor who is use to short term contracts.

POSITION TITLE:  Clinical Trial Manager

DIVISION: Pharma Services- Clinical Operations

DEPARTMENT:  Project Management

LOCATION: Home-based position anywhere within the US

REPORTS TO: Senior Director, Clinical Operations            

JOB STATUS:  Contract



The Clinical Trial Manager (CTM) is responsible for supporting the coordination of  clinical study management activities, study startup activities including site selection, study team management, and project timelines for the CRO. The CTM works closely with and supports the PM, the funder, sponsor, investigator, and appropriate staff in each department of the company including medical writer, data management, site management, quality assurance, contracts, and scientists as needed to help launch and complete the study.  The CTM will assist in the management of the trials and sites, and have responsibility for assisting the PM with timelines and budget adherence with each trial. The CTM also works closely with the PM and CTS during study startup to manage site feasibility and selection process.  As part of the site management responsibilities, the CTM manages the CRA activities along with the PM, reviews trip reports as needed, and may assist with the performance of site qualification, site initiation, co-monitoring and/or close-out visits as needed. The CTM is responsible for demonstrating professional demeanor and maintaining confidentiality in all interactions with both internal and external contacts.  Work is performed under the general direction of the Senior Director, Clinical Operations.


Assist in the Development, Implementation, and Management of Research

Studies,areas of which might include:

o    Determining site selections through feasibility questionnaire process

o    Oversight of  protocol administration including pre-study work, initiation of sites,  ongoing  progress of trial and close out of sites

o    Implementation of action plans to keep project on track

o    Oversight and ensured delivery of project deliverables

o    Working with the CRAs to ensure site protocol adherence and query resolution

o    Working with the CRAs to review trip reports and corresponding expense reports, by project, as assigned or upon request

o    Assisting the PM in the training of CRAs on the protocol and the science of the trial

o    Helping to train data management on protocol and may work with the data management group throughout the trial to include assistance with CRF development, ongoing queries and data lock procedures

o    Assist with ongoing site management including interim calls to sites, addressing clinical questions from sites and CRAs in the field, and trouble-shooting as needed

o    Effective communication of protocol issues/status to all departments

o    Assist in preparing accurate reports to PM as needed

o    Assist with ongoing review of data as needed

o    Continue to assist in development of processes with the growth of the area and incorporating those processes with other departments

o    Assist the PM in developing relationships with funders or sponsors

o    Participates in departmental meetings with project management, finance, site management, data management, and biostatisticians

o    Participates in pharmaceutical meetings as needed

o    Helps PM to set and manage regularly scheduled meetings with key staff

o    Helps to develop timelines based on project priority list

Please call me now on 919-838-7478 or email

Contact Details:
Tel: 919-838-7478
Contact: Ben Henning

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