Clinical Trials Manager

Location:San Mateo - United States
Salary:Highly Competitive Salary
Reference No:CR.CF.13179
Already a member? Login  |  Create Account

An exciting opportunity has arisen for a Clinical Trials Manager to join a global biopharmaceutical company based in San Mateo, CA. A very patient-focused company, who scientific research has resulted in 15 marketed products that are benefitting hundreds of thousands of people, a pipeline of late-stage drug candidates and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them.  

Job Responsibilities:

  • Must meet all requirements for Principal Clinical Research Associate position and have demonstrated proficiency in all relevant areas.
  • In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines.
  • Coaches members of a work team and ensures adherence to established guidelines.
  • Provide input to program budget and timelines to ensure successful management of all aspects of international clinical trials.
  • Anticipates obstacles and client difficulties and implements solutions to achieve project goals.
  • Assists CPM in revising project timelines/budgets as necessary.
  • Works with management on departmental issues, providing input to clinical operations strategies and work plans.
  • Communicates with functional peers regarding project status and issues and ensure project team goals are met.
  • Contributes to development of abstracts, presentations and manuscripts.
  • Participate in the recruiting and hiring process for CPA/CRAs and support their professional development.
  • Participate in training of CPAs and CRAs.
  • Provide guidance and training to CROs, vendors, investigators, and study coordinators on study requirements.

Skills and Requirements:

  • Excellent interpersonal skills and demonstrated ability to lead is required.
  • Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction.
  • Strong communication and influence skills and ability to create a clear sense of direction is necessary.
  • Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction.
  • Must have a demonstrated ability to successfully develop, implement, manage Clinical Trials.
  • Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is required.

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 Christopher Frank on +1 267 405 6996 or upload your resume on our website -
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.

Useful Links

Enter your email below to subscribe to our weekly newsletter: