OPIS is looking for a skilled and experienced CRA Line Manager in the EU.
This is a remote, home-based role in Spain.
The Clinical Research Line Manager provides leadership and supports the Clinical Research Associate (CRA) team in executing clinical trials at a local and global level, ensuring client projects are delivered efficiently, with high quality, and in compliance with the contract's requirements.Some of what you'll do: Coordinate and oversee day-to-day activities of the CRAs, ensuring the highest performance, quality, and efficiency.Ensure effective CRA allocation, project-specific training, and overall smooth execution of CRA activities in relation to the agreed KPIs.Assist the CRAs in issue resolution and proper escalation, ensuring that the corrective action plan is put in place within the agreed timeframes.Plan and hold regular meetings with CRAs, accompany them on site visits, perform TMF checks, and review monitoring visit reports.Ensure a proper and timely handover in case of CRA change.Identify any team performance issues and define the corrective action plan.Ensure that Sponsor's systems are updated by the team within the required timelines.Ensure that documents and correspondence are properly archived and the Trial Master File is inspection-ready.Maintain contacts with the Sponsor and participate in meetings and teleconferences.Collaborate in maintaining the SOPs related to his/her area of activity.Perform monitoring activities for sites allocated to him/her, if needed.Collaborate with other colleagues involved in the projects to ensure management of the full project lifecycle in compliance with regulations, quality standards, procedures, and policies.Motivate the team and encourage team members to be proactive, increase efficiency, take initiatives, and share concerns.Cooperate to hire and train new associates and act as a mentor for junior staff.Requirements: Enthusiasm, knowledge, and proactivity.Degree in a scientific field.At least 5 years in the clinical research field with proven line management experience.Excellent knowledge of GCP.Able to coordinate all activities related to site management and monitoring of clinical trials both locally and internationally.Effective interpersonal skills with excellent customer service and team leadership skills.Excellent knowledge of the English language.Good ability to interact with colleagues and clients.We offer a competitive salary with other benefits and the opportunity to develop your professional career with a growing company.#J-18808-Ljbffr