Clinical Trial Associate Job

CLINICAL TRIAL ASSOCIATES needed for CONTRACT opportunities with Yoh's client located in Danbury, Connecticut.

THE BIG PICTURE - TOP SKILLS YOU SHOULD POSSESS:

- CTMF (Clinical Trial Master File) proficiency
- Clinical trial experience
- Pharmaceutical industry experience
- Clinical trial documentation

WHAT YOU'LL BE DOING:

- Ensures all trial documentation is prepared, accurately filed and saved into CTMF. Liaise with trial personnel to follow-up on required documentation.
- Prepares and distributes Investigator Site File (ISF) to sites.
- Prepare CTMF documents for inspection readiness.
- Coordinate with Document Management System support staff to ensure appropriate data dictionaries are updated for new trials.
- Reconciles trial documents throughout the trial in preparation for trial close-out.
- Assists in Clinical Trial Report preparation by linking appendices with Document Management System.
- Coordinate with Document Management System support staff to ensure appropriate data dictionaries are updated for new trials.
- Reconciles trial documents throughout the trial in preparation for trial close-out.
- Assists in Clinical Trial Report preparation by linking appendices with Document Management System.

WHAT YOU NEED TO BRING TO THE TABLE:

- Experience supporting clinical trial teams.
- CTMF (Clinical Trial Master File) experience.
- Document management.
- Understanding of Regulatory Compliance and Record Retention policies.
- Solid understanding of Clinical Trial Master File requirements, Good Clinical Practices, and SOP's, document management system functionality and practices.

OPPORTUNITY IS CALLING, APPLY NOW!

RECRUITER: Vera Evan

PHONE NUMBER: Yoh, a DayJ2W: CLINICAL

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