Clinical Monitoring Jobs/Site Management Jobs

Kforce offers a variety of options from routine monitoring to full-site management.  Specific job definitions and responsibilities vary by sponsor company. 

• Coordinate effective communication between Investigative Sites, as well as Study Management and Data Management teams
• Manage multiple investigational sites for multiple protocols covering different therapeutic areas
• Ensure investigational sites maintain requisite regulatory and study specific documentation and are aware of their obligations
• Ongoing supervision of investigative sites to assess compliance with protocol, sponsor, GCP and regulatory requirements in order to ensure the safety of subjects and accuracy of data
• Conduct pre-study, site initiation, interim monitoring, and study closeout visits and complete associated reporting requirements in accordance with SOPs
• Review CRFs (or EDC) and verify completeness and accuracy via source document verification activities
• Drive investigator selection process, patient recruitment strategies and enrollment plans

Skills:

• Bachelor's degree, preferably in a scientific or nursing discipline
• A minimum of 2 years experience in a biopharmaceutical or CRO setting functioning as a CRA
• Hands-on experience with study start-up, interim, and closeout activities
• Strong communication skills
• Interact effectively with many different personalities and/or team members who are not collocated
• Ability to work independently

Search Clinical Trial Monitor and Site Management Jobs Now.

You can also contact a Kforce team member at ClinicalResearch@Kforce.com or call us at 1-877-4KFORCE.

*Job responsibilities and skills required will vary across hiring organizations