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Open nowFirst seen 6 days ago

Remote Women's Fertility Clinical Research Associate III

global-channel-management-inc944 open roles

Where
Atlanta, Georgia, United States, Remote
Work mode
Remote
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Your applicationOpen nowRemote Women's Fertility Clinical Research Associate IIIglobal-channel-management-inc · Atlanta, Georgia, United States, Remote

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.7%14 days
  5. 35.6%30 days
  6. 58.0%60 days
This job: first seen 6 days ago

The posting

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 escalate 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:

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

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