Manager, PV – Medical Project Coordinator Team

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Manage multiple aspects of projects, both local and globally, such as contractual, procedural and regulatory requirements. • Maintain good communications with other functional groups concerning program and company issues. • Collaborating with other employees in problem solving and systems improvement. • Review regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices, procedures and proposals. • Maintain a basic medical understanding of applicable therapeutic areas and disease states. • May participate in on-call duties for specific projects and ensure 24-hr coverage for intake of cases from investigative sites. • Provide plans and accurate forecasts for all projects. • Serve as a resource for other departmental managers and lead departmental initiatives. • Prepare and present proposals. • Manage staff of experienced professionals, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring, employee counseling, and separations. Approve courses of action on salary administration, hiring, corrective action, and terminations. • Review and approve time records, expense reports, requests for leave, and overtime.

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification to include 3+ years of safety experience • Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 5+ years). • 1+ year of leadership responsibility • Working knowledge of the global regulatory requirements and the importance of and compliance with procedural documents • Strong knowledge of relevant therapeutic areas as required for processing AEs • General knowledge of pathophysiology and the disease process • Time management and project management skills • Proficiency in Microsoft Office products and safety databases • Good command of English and ability to translate information into local language where required • Excellent oral and written communication skills • Strong attention to detail and accuracy • Strong critical thinking, problem solving and decision-making skills

🏖️ Benefits

• Flexible work arrangements • Professional development opportunities