Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Position Overview: We are seeking a highly skilled and experienced professional in Europe to oversee clinical pharmacology deliverables and serve as an ESA Subject Matter Expert (SME). The ideal candidate will have a strong background in medical writing, peer review, and coaching, with specific expertise in early phase protocol development and ESA management. Key Responsibilities: Clinical Pharmacology Oversight: Oversee the development and delivery of clinical pharmacology deliverables, including but not limited to 2.7.1, 2.7.2, and ESAs. Conduct peer reviews and provide coaching to writers to ensure high-quality outputs. Experience of managing early phase assets. Act as the primary point of contact for planning and resourcing ESA requests. Lead the development of clinical pharmacology RACIs and establish effective ways of working. Support the development and rollout of early phase protocol including developing/refining long-term monitoring, feedback, and update plans. Serve as a medical writing reviewer for clin pharm template updates. Review clin pharm documents to ensure compliance with client style guides. Pilot and assess the capabilities of medical writers to lead clin pharm documents. Key Requirements: Proven experience in clinical pharmacology deliverable oversight and medical writing. Expertise in ESA management and protocol development. Strong leadership and coaching skills. Excellent communication and organizational skills. Ability to work collaboratively with cross-functional teams. Familiarity with early phase clinical studies and regulatory requirements. Preferred Experience: Working in an FTE role. Thank you for your interest as you consider starting a new career journey with us. As the world leader in serving science, our colleagues develop critical solutions through innovation—and build rewarding careers. Discover their extraordinary stories and connection to our Mission to enable our customers to make the world healthier, cleaner and safer. Their work is a story of purpose. What story will you tell? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.