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Data Management Specialist

2 weeks ago

Remote, Canada Centricity Research Full time

Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research.

The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic clinical trials in a variety of therapeutic areas throughout phases 1-4. The sites that were formerly known as IACT Health brings phase I-IV clinical trials in over 30 therapeutic areas such as oncology, cardiology, pulmonology, endocrinology, infectious disease, and pain with wholly owned and integrated clinical research offices in multiple cities in the United States across the Southeast, including Georgia and Virginia. The sites that were formerly known as LMC Manna bring phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence big data research, vaccine research, and primary care studies within Canada at sites across Alberta, Ontario, and Quebec. The sites that were formerly known as True North Clinical Research are located in Nova Scotia and specialize in research related to Alzheimer’s disease and conditions related to aging, and are committed to finding new treatments to maintain an improved quality of life for patients through innovation and passion.

Centricity Research is committed to revolutionize research by creating outstanding clinical trial experiences to improve the health of the community today and tomorrow through clinical research.

Currently, our rapidly expanding team and site network is looking for a Data Management Specialist** **who can work for us on a** full-time, temporary basis** supporting our sites **remotely.**

**Responsibilities will include but are not limited to**:

- Gain familiarity of protocols and case report forms
- Perform accurate, complete, and timely data entry of case report forms (CRFs) & timely query resolution
- Meet data entry and query timelines as identified by sponsor
- Highlight any missing information and/or errors in source documents
- Assist CRPs in responding to data management queries, monitor findings, and follow-up
- Support continued QC in the creation and maintenance of source documents, highlighting edits needed
- Stay in constant communication with CRC and CRA to stay up to date with any new study related information.
- Obtain, process, copy, scan, and file documents, as required
- Process signed results and file, as required
- Abide by GCP, SOPs, company guidelines, and local healthcare privacy regulations
- Perform other administrative tasks as required by CRPs and Research Management

**Requirements**:

- If in Canada: College diploma/University degree in a relevant field of science is required
- If in the US: High School/GED
- At least 2 years’ experience in an administrative role
- Experience working with multiple teams in a collaborative environment
- Previous experience in a health care environment preferred

**Centricity Research** is committed to meet the accessibility needs of persons with disabilities in a timely manner. These accommodations will be available upon request.

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