Clinical Trial Manager

Clinical Trial Manager
  • $1 - $2 per Hour
    HOUR
  • Permanent
  • Cambridge MA, US Cambridge Cambridge US 00000
Job Ref: JO000109181
Sector: Clinical
Sub-sector: Clinical
Date Added: 15 February 2021

Clinical Trial Manager - REMOTE

SRG is seeking a Clinical Trial Manager responsible for the successful planning, implementation and execution of clinical monitoring activities to supporting a growing midsize biotech. Functionally responsible for all clinical monitoring team members throughout the duration of each clinical trial. Assures clear vendor and internal team communication, process documentation, and compliance with Good Clinical Practices. This is a REMOTE - Direct Hire opportunity.

KEY RESPONSIBILITIES

The Clinical Trial Manager will assist in the following day-to-day tasks including but not limited to:

  • Work with Study Manager to define program targets for clinical monitoring staff.
  • Develop and implement Clinical Monitoring Plan.
  • Develop site/monitoring tools and training materials.
  • Review and identify trends in data entry at sites and proactively interface with clinical monitoring team and client to identify solutions.
  • Set and enforce project timelines with the assigned study team.
  • Coordinate remote review of clinical data within EDC system.
  • Oversee monitoring visit schedule to ensure compliance in Clinical Monitoring Plan.
  • Approve trip reports and follow-up letters within required timeframe.
  • Schedule and manage weekly CRA project team meetings.
  • Ensure CRAs assigned to team receive therapeutic and project-specific training.
  • Assure that the appropriate SOPs are followed and all project documentation is appropriately filed
  • Manage quality and regulatory compliance among clinical monitoring team and investigational sites.

PROFESSIONAL EXPERIENCE/QUALIFICATIONS

  • Minimum of 2 -3 years as a successful Clinical Trial Manager.
  • Prior experience as a Clinical Research Associate.
  • Thorough knowledge of clinical research process.
  • Knowledge of FDA regulations and their practical implementation.
  • Strong verbal and written communication skills.
  • Proficient computer skills including Microsoft Office Word, Excel and Power Point.
  • Ability to manage and prioritize workload effectively.
  • Willingness and ability to travel domestically and internationally, as required.

EDUCATION

  • University or college degree, or certification in a related health profession

SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

SRGTalent
13/03/2021 12:00:00
USD 1.00 2.00 Hour
Contact Consultant:
Melissa Rodrigues

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