Clinical Research Manager

1 week ago

Vaughan, 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.

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 an **Clinical Research Manager **who can work for us on a** full-time, permanent basis**, supporting our **Vaughan** and** Barrie** locations.

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

- Manage quarterly recruitment targets and support efforts to achieve site/company KPIs
- Support admin to verify operations metrics are available and accurate
- Support in recruiting and hiring of staff
- Train employees and model continuous improvement
- Conduct reviews/check-ins as outlined by HR
- Approve time off request and timecards
- Supervise, train, mentor and develop staff
- Provide ongoing feedback and coaching to all staff
- Transparency with the organic growth and future of the company
- Anticipate issues and needs for the site based on trends seen at the site level
- Actively develop and seek opportunities for regional and site-specific growth
- Serve as a resource for all teams
- Fostering cohesiveness at all levels of the company
- Unify site specific culture and Centricity fundamentals
- Ensure the safety and welfare of study participants
- Conduct the study as per protocol, GCP, and SOPs including screening study participants based on protocol inclusion/exclusion, scheduling visits, and obtaining study specific assessments e.g. vitals
- Perform delegated research and administrative procedures to assist in conducting clinical studies under the direction of the Investigator
- Perform ECGs, vital signs, meal distribution, study participant monitoring, and other tasks as required by protocol/site
- Verify input data and timely documentation regularly and accurately
- Support the review of source docs and other study documents
- Perform regular quality control (QC) checks and other QC tasks as deemed necessary
- Support feasibility review and submissions, where required
- Conduct/support PSV
- Support audit preparation for any site inspections
- Abide by GCP, SOPs, company guidelines, and local healthcare privacy regulations
- General site level support

**Requirements**:

- Minimum 2 years working in clinical research
- Minimum 1 year of management experience
- Valid drivers license and reliable access to a vehicle is required
- College or university degree in life sciences or related field preferred
- Post-secondary education in a clinical research program would be an asset
- Certification through the Association of Clinical Research Professionals (ACRP) would be an asset

**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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