Labcorp Hiring for Clinical Trial Coordinator at Princeton, NJ Full Time

Clinical Trial Coordinator – FSP Sponsor Dedicated

Remote – USA

Essential Job Duties:

• Collect, track and perform a quality review of all essential & investigator documents required for effective and compliant study site activation and maintenance
• Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines
• Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.
• With guidance from line manager and experienced colleagues, adapt Informed Consent Forms and other patient facing material to country specific requirements.
• May support / assist the contract negotiation process under supervision of an experienced colleague or line manager.
• Escalate study issues appropriately and in a timely fashion.
• Update study documents when there are changes in study personnel/study amendments.
• Contribute to the preparation of submissions to IRB/IEC with appropriate supervision.
• Ensure high quality documents are filed and systems are updated on an ongoing and timely basis making Covance ready for an audit at any time.
• Undertake tasks delegated by senior team members, depending upon country and situational requirements with proper supervision.
• Perform other duties as assigned by management.

Education/Qualifications:

• Bachelors Degree is preferred (but not required)

Requirements:

• 1 – 2 years in clinical research

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant’s race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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