Medical Project Coordinator

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

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

• Coordinate and review safety data using line listings, company dashboards, and visualization tools • Review data for safety trends, coding consistencies, and potential investigator-site follow-up • Identify potential issues and resolve or escalate them appropriately • Review safety data and provide summations for safety review meetings • Review designated sections of aggregate reports • Help create and review safety and medical management plans for studies • Ensure plan processes reflect contracted services • Help manage routine project implementation, forecasting, and coordination, including metrics and budget considerations • Monitor data-review status and escalate delays or risks to stakeholders and study leads • Present at business development, client, and investigator meetings • Participate in strategy and business development calls • Resolve complex problems through in-depth evaluation and offer solutions • Serve as primary contact for clinical/data management project teams • Assist management with training and mentoring

🎯 Requirements

• Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN • 2+ years of relevant experience • 2+ years of clinical safety experience in clinical research monitoring, pharmacovigilance, or a combination of both • Equivalency through appropriate education, training, and/or directly related experience may be considered • Knowledge of GCPs for medical oversight of clinical trials and SAE processing • Knowledge of drug development and safety reporting • Knowledge of safety data trending, including coding • Working knowledge of biostatistics, data management, and clinical procedures • Strong problem-solving and critical-thinking skills • Good oral and written communication skills • Good attention to detail • Ability to work in a collaborative team environment • Ability to maintain a positive and professional demeanor in challenging circumstances • Ability to work in an upright and/or stationary position for 6–8 hours per day • Ability to perform repetitive hand movements and frequent mobility • Ability to lift and carry 15–20 lbs • Ability to access and use in-house and off-the-shelf computer software • Ability to communicate and understand spoken and written information • Ability to perform under stress and multitask • Regular and consistent attendance

🏖️ Benefits

• Collaboration and development as part of the everyday experience • Reasonable accommodation for individuals with disabilities during application, interview, and essential job functions • Equal employment opportunity