Covance Senior CRA Manager - France in France

Job Overview

Covance is looking for an experienced home-based CRA Manager to lead a team of 12 CRAs across France.

Successful applicants will ideally have between 3-10 years of previous CRA management experience of CRAs and will be based in France. We are hoping to find applicants in the Paris or North West region of France but may consider other locations.

Responsibilities:

Has GCP Oversight of direct reports by ensuring GCP training is executed, understood and implemented

Identify and escalate GCP issues identified through regular interactionswith direct reports and conduct of Quality Control Visits

Ensures training record compliance with training matrix and ensure

Hold clinical operations and co source saff accountable for GCP issue escaliation to the management team, the sponsor and QA, as appropriate.

Coach assigned staff to own effective investigator relations and investigator oversigh at the local level.

Communicate status of assigned workload for metric reporting

Perform weekly review of direct report biliable hours and associated utilization per the quaterly and annual budget plan, and escalation of outliers to management team for mitigation.

Escalates availaleworkload jours, in contact of project allocation, supply and demand, to management team.

Engage in Resource management activities for direct reports.

Schedule Quality Control visits to ensure costs are in alignment with regional budget.

Education / Qualifications

Required :

University/college degree - life sciences preferred or certification in a related allied health profession from an appropriately accreditedinstitution.

In lieu of this required educational backgroung the following relevant work history may be considered :

Minimum of 3 years supervisory experience in a health care or clinical reserach srtting and

Minimum of seven years relevant clinical research expericne in a pharmaceutical company/CRO

Preferred : Masters or other advanced degree.

Experience

Relevant clinical research experience in a pharmaceutical company or CRO

Individual is proficient with on site monitoring activities

Minimum of 5 years relevant clinical research experience in a pharmaceutical company/CRO

Thorough knowledge of drug development process

Thorough knowledge ofrelevant SOPs, ICH, and GCP guidelines

Relevant supervisory experience

Minimum of 1year as a line manager or project manager required

Demonstrated abilityto lead by exampleand to encourage teammembers to seeks solutions.

Proven interpersonal skills.

Advanced oral, written and presentation skills

Advances planning and organizational skills.

Job Number 2018-20568

Job Category Clinical Operations

Position Type Full-Time

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.