Clinical Project Manager job in Irvine, California

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This vacancy has now expired. Please see similar roles below...

At Proclinical, we are seeking a talented individual to fill the role of Clinical Project Manager, based in Irvine, CA.

Responsibilities

Clinical study execution in support of the Client's team and their overall Clinical Center of Excellence with a focus primarily on clinical cardiovascular studies.
Serve as a member or leader of the study core team and may serve as the liaison with the operating company for projects under his/her responsibility.
Lead several clinical studies (regulated and non-regulated).
Manage large regulated studies alongside and in support of colleagues and management.
Identify and ensure strategies, resources, and accountabilities are in place.
Manage all activities of assigned clinical studies within the Clinical R&D Operations group.
Evaluate support requests for publications.
Manage resources assigned to designated clinical studies.
Track assigned projects budgets to ensure adherence to business plans.
Support implementation of new clinical systems/processes. Provide support for publications.
Interface and collaborate with investigators, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel.
Ensure compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance.
Provide quality feedback to management on each resource assigned to clinical studies.

Skills And Qualifications

BA in Life Science, Physical Science, Nursing, or Biological Science preferred, and 5+ years of experience required as Clinical Project Manager, as well as 1+ years of Clinical Project Management experience.
Cardiovascular clinical trial experience strongly preferred.
Personnel management experience strongly preferred.
Medical device experience is preferred.
The ability to influence others along with strong written and oral communication skills is required.
Knowledge of Good Clinical Practices is required.
Understanding and application of regulations and standards applied in clinical areas is required.
Strong written, verbal, and interpersonal communication skills.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Samantha Reader at (+1) 267-983-0134 or upload your resume on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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