Senior Medical Project Coordinator

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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, coordinate and evaluate medical projects for one or more programs in collaboration with management and other stakeholders. • Work independently to perform first pass review of safety data, utilizing line listings, company dashboard(s) and/or other visualization tools. • Review safety data and provide summations for safety review meetings. • Independently function as the Project Lead for medical monitoring services when SAE case processing has not been contracted. • Create and maintain medical management plan(s) on studies. • Work independently to monitor the project financial status, unit forecasting, actual realization, and team allocations in systems. • Resolving complex problems through in-depth evaluation of various factors and offers solutions. • Present at business development, client, and investigator meetings and participates in strategy/business development calls.

🎯 Requirements

• Bachelors degree in Nursing or related Health Sciences (Physician's Assistant) or licensed RN • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years) • 5+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance) • Advanced knowledge of GCPs for medical oversight of clinical trials • Knowledge of drug development and safety reporting • Advanced knowledge of safety data trending to include coding • Working knowledge of biostatistics, data management and clinical procedures • Excellent problem solving and critical thinking skills • Excellent project management and budget skills • Effective mentoring skills and ability to train and lead others • Strong oral and written communication skills • Strong attention to detail • Ability to work in a collaborative team environment • Ability to maintain a positive and professional demeanor in challenging circumstances

🏖️ Benefits

• Health insurance • Retirement plans • Paid time off • Flexible work arrangements • Professional development