Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.

• Manages multiple aspects of projects, both local and globally, such as contractual, procedural and regulatory requirements.
• Maintains good communications with other functional groups concerning program and company issues. Collaborates with other employees in problem solving and systems improvement.
• Reviews regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices, procedures and proposals.
• Maintains a basic medical understanding of applicable therapeutic area and disease states.
• Provides plans and accurate forecasts for all projects.
• Serves as a resource to other departmental managers and leads departmental initiatives. Prepares and presents proposals.
• Manages 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. Approves courses of action on salary administration, hiring, corrective action, and terminations. Reviews and approves time records, expense reports, requests for leave, and overtime.

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification to include 3+ years of safety experience
• Previous experience that provides 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
• Proficient 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