Clinical Trial Manager

Clinical Trial Manager
  • $65 - $85 per Hour
    HOUR
  • Temporary
  • CAMBRIDGE MA, US CAMBRIDGE MIDDLESEX US 02139
Job Ref: JO000127316
Sector: Science
Sub-sector: Food & FMCG
Date Added: 06 January 2022

Clinical Trial Manager

6 month contract possible renewal

Description:

Job Description
The Role:
The Clinical Trial Manager provides clinical trial oversight to the assigned clinical trial(s) ensuring deliverables are met in terms of quality, compliance and timing. Strong vendor management is critical for this role. external vendors and CROs.The position reports to the Director, Clinical Operations and is accountable to the Clinical Operations Lead for assigned studies.This role may work collaboratively on one trial or across several trials to support clinical operations activities.
Here’s What You’ll Do:

  • Day to day management of assigned clinical trial(s) to ensure deliverables are met in all phases of trial
  • Communication to internal team members on deliverables and ensuring timelines are met
  • Manage trial feasibility process
  • Work closely with study Clinical Operations Lead and/or assigned Clinical Trial Manager(s) to execute clinical studies
  • Drafting site materials including training, manuals and support documentation
  • Monitoring of clinical data to ensure timely entry and readiness for data review meetings
  • Periodic review of clinical data
  • Review of clinical monitoring reports to ensure timely completion and identification of issues
  • Ensure trial samples are ready to be sent to vendors in order to meet trial deliverables
  • Maintain trial metrics
  • Ensure trial is conducted in accordance with Moderna and ICH/GCP standards including multiple regions in global trials
  • Support testing clinical trial systems/databases (i.e. UAT)
  • May support additional clinical trial(s) in an unblinded Clinical Trial Manager capacity
  • Develop and maintain strong, collaborative relationships with key stakeholders within Moderna

Here’s What You’ll Bring to the Table:

  • At least 5 five years of trial coordination experience in a clinical research and industry environment
  • Advanced degree preferred or Bachelor’s in a science-based subject
  • Relevant experience in global setting
  • Solid understanding of drug development
  • Good project management skills
  • Good understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies
  • Excellent verbal and written communication skills
  • Good organizational skills and attention to detail

#LI-KR1

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
06/02/2022 12:00:00
USD 65.00 85.00 Hour
Contact Consultant:
Katherina Ramirez

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