Remote Women's Fertility Clinical Research Associate III
Atlanta, Fulton County, Georgia, 30383, USA
Listed on 2026-01-12
-
Research/Development
Clinical Research, Research Scientist -
Healthcare
Clinical Research
Remote Women's Fertility Clinical Research Associate III About the job Remote Women's Fertility Clinical Research Associate III
Remote Clinical Research Associate III needs 2 years of site management and field monitoring experience
Remote Clinical Research Associate III requires:
Work Schedule:
M-F 7:00 am
-3:30 pm or 8:00 am to 4:30 pm
EST
Qualifications:
BS/BA
Minimum of 2 years of site management and field monitoring experience
Knowledge of applicable standards and regulations for clinical trials
Proven oral and written communication skills
Proven planning skills; ability to create and track detailed project plans
Proven interpersonal, leadership, organizational and effective time management skills
Demonstrated experience in computer skills to include Microsoft Word, Excel and basic templates
Ability to work independently and within a cross-functional team environment to identify and elevate site/monitoring related activities issues to the management team in a timely fashion
Preferred:
- Experience in womens fertility
- VD Study Experience
- Medidata RAVE system
Remote Clinical Research Associate III duties:
Verifies required clinical data entered in the electronic case report form (eCRF) is accurate and complete
Manages site communication and escalates to leadership in a timely fashion when needed
Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines
Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF).
Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.
Documents activities via confirmation letters, follow-up letters, trip reports
Site support throughout the study lifecycle from site identification through close-out Attends and participates in internal meetings
#J-18808-Ljbffr(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).