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
To learn more about our current clinical monitoring / site management jobs, click on one of the current opportunities below.
|
Regional Clinical Research Associate
|
Cincinnati, OH
| Contract |
|
Regional Clinical Research Associate
|
Chicago, IL
| Contract |
|
IH Clinical Research Associate (CRA)
|
Murray Hill, NJ
| Direct Hire |
|
Regional Clinical Research Associate
|
Dallas, TX
| Contract |
|
Regional Clinical Research Associate
|
Seattle, WA
| Contract |
|
Regional Clinical Research Associate
|
Boston, MA
| Contract |
|
Regional Clinical Research Associate
|
Memphis, TN
| Contract |
|
Regional Clinical Research Associate
|
Denver, CO
| Contract |
|
Clinical Research Associate
|
San Francisco, CA
| Direct Hire |
|
Regional Clinical Research Associate
|
Orlando, FL
| Contract |
|
Regional Clinical Research Associate
|
Milwaukee, WI
| Contract |
|
Regional Clinical Research Associate
|
Los Angeles, CA
| Contract |
|
Regional Clinical Research Associate
|
Detroit, MI
| Contract |
|
Regional Clinical Research Associate
|
Baltimore, MD
| Contract |
|
Regional Clinical Research Associate
|
Atlanta, GA
| Contract |
|
Regional Clinical Research Associate
|
Indianapolis, IN
| Contract |
|
Regional Clinical Research Associate
|
Lexington, KY
| Contract |
|
Regional Clinical Research Associate
|
Louisville, KY
| Contract |
|
Regional Clinical Research Associate
|
Columbus, OH
| Contract |
|
Regional Clinical Research Associate
|
Minneapolis, MN
| Contract |
|
Regional Clinical Research Associate
|
Cleveland, OH
| Contract |
|
Regional Clinical Research Associate
|
Philadelphia, PA
| Contract |
|
Regional Clinical Research Associate
|
Phoenix, AZ
| Contract |
|
Regional Clinical Research Associate
|
Hartford, CT
| Contract |
|
Regional Clinical Research Associate
|
Akron, OH
| Contract |
You can also contact a Kforce team member at mlee@kforce.com or call us at 1-877-4KFORCE.
*Job responsibilities and skills required will vary across hiring organizations