global channel managementAtlanta, GA
Remote Women's Fertility Clinical Research Associate III
Remote Women's Fertility Clinical Research Associate III
Remote Women's Fertility Clinical Research Associate III
global channel managementAtlanta, GA
8 days ago
Clinical Research CoordinatorsClinical Data ManagersFirst-Line Supervisors of Farming, Fishing, and Forestry Workers
Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)Other Scientific and Technical Consulting ServicesAll Other Outpatient Care Centers
Apply for this role →Remote Women's Fertility Clinical Research Associate IIIAtlanta, Georgia, United States$ 49.00 - 50.00 (US Dollar) 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 pmEST
Qualifications:
- BS/BAMinimum 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 escalate site/monitoring related activities issues to the management team in a timely fashion
Preferred:
Experience in womens fertilityVD Study Experience
Medidata RAVE system
Remote Clinical Research Associate III duties:
- Performs Site initiation, interim & close out monitoring visits
- 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
Also on the board Same function, level within a rung
Level
Senior
Location
Atlanta, GA
Occupation
Clinical Research Coordinators
Industry
Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
Posted
8 days ago