Clinical Project Manager

Proclinical Staffing are proud to be partnered with leading CRO in the industry who are searching for an experienced Freelance Clinical Project Manager - Single Sponsor to join the team. This is a contract role with the duration of 12 months.
Responsibilities: Oversight and operational management of clinical Trials from study design until study close-out, ensuring on time and on budget completion, with adherence to the required quality standards and compliance with ICH, GCP and Company's Standard Operating Procedures (SOPs).Design and development of full synopsis and protocol by leading cross-functional team members.Manage timely and accurate documentation and communication of trial progress.Management of study budget, scope changes and financial reconciliation.Oversight of selected vendors and status of related deliverables.Preparation and coordination of scientific meetings incl. KOLs meeting, Investigators' meeting, blinded review meeting.Attend and lead bid defense meetings.Key Skills and Requirements: Minimum of 3 years Clinical Project Management experience.Strong background working for CROs.Good experience with bid defenses and working on clinical trials across phases I - IV.Oncology experience.If you are having difficulty in applying or if you have any questions, please contact Sam Rodriguez at ******.
Apply Now: If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV.

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