CRA/ Sr CRA - Clintec position - Single Sponsor

We are lookingtorecruitcommittedindividualstowork in a busyclinicalresearchdepartmentprovidingessentialmonitoringsupport.The role providestheopportunitytodevelopmonitoringskillswithadvancedresponsibilities, critical and central totheconductoftheclinicalproject.The CRA overseestheprogressof a Clinical Trial, ensuringthatitisconducted, recorded and reported in accordancewiththeprotocol, Standard OperatingProcedures (SOPs), Good ClinicalPractice (GCP) and theapplicableRegulatoryrequirements

While projects vary, your typical responsibilities might include: 

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation

• Supporting the development of a subject recruitment plan

• Establishing regular lines of communication plus administering protocol and related study training to assigned sites

• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate

• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution 

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

Qualifications:

• A Bachelor's degree in a health care or other scientific discipline or educational equivalent

• At least 2 year of experience as a CRA

• Preferably with oncology experience.

• Location: Flexible

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team. 

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