Job Overview : WHO ARE WE?
WHO ARE WE?
As a leading contract research organization (CRO), Labcorp Drug Development (formerly known as Covance) provides comprehensive drug development solutions for a range of industries.
Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.
Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services.
Our unique perspectives are based on decades of scientific, medical and regulatory expertise.
We are recruiting for our FSPx business in Greece and are currently seeking to hire a Line Manager, Clinical Operations with a permanent and full-time contract .
Responsibilities include but are not limited to :
Responsible for the supervision of assigned direct reports within FSP team
Responsible for detailed performance review and management of assigned direct reports including : Annual Performance Management and Development (PMD), Individual Development Plan (IDP), Line of Sight Goals and "Shoves & Tugs"
Responsible for appropriate management and resolution of performance issues
Measure performance indicators for assigned staff
Escalate potential individual training needs and assist in the conduct of training and develpment efforts, regionally
Conduct, report and follow-up on Quality Control Visits (CQC)
Effectively communicate management strategies, policies and procedures in conjunction with leadership teams
Develop and maintain effective relationships with management team to manage assigned staff in a matrix environment
Maintain good working relationships with internal and external clients to ensure opportunity for acquiring additional new business
Education / Qualifications :
University / college degree - life sciences preferred or certification in a related allied health profession from an appropriately accredited institution (e.
g., nursing certification, medical or laboratory technology)
Previous relevant work experience
Demonstrate excellent problem solving skills, a proactive approach and the ability to make sound decisions
Demonstrated skill in leading teams, by example and mentoring staff
Excellent oral and written communication and presentation skills
Knowledge of clinical trial process
Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies
Demonstrated ability to work in a team environment
Demonstrated ability to handle multiple competing priorities
Proven managerial and interpersonal skills
Fluency in Greek and English