
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.
🔥 0 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Accountable for achieving the final clinical deliverable (usually clean data from valuable patients as specified in the study protocol) within the time period specified in the contract with the customer • Interprets data on project issues and makes good business decisions with support from expert team members or line manager • Manages all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP • Develops clinical tools (e.g. Supervising Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan • Contributes to the development of the Master Action Plan (MAP) for providing clinical related documents • Ensures timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central) • Collaborates with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings • Regularly communicates with the team and leads team meetings to ensure that timelines, resources, interactions, and quality are maintained • Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies • Responsible for the timely archiving of documents and study materials for the department
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides knowledge, skills, and abilities to perform the job (comparable to 8+ years) • PREFERRED therapeutic indication experience: Ophthalmology (General ophthalmology, Diabetic Macular Edema & Geographic Atrophy), Rare Disease (Myasthenia Gravis, Huntington's, ALS, DMD, CIDP, DM1 (myotonic dystrophy) and FSHD - CAR-T experience a plus), Sleep, Epilepsy, and/or Psychiatry • PREFERRED experience level: 3+ years of CTM experience (North America) + global gCTM experience +/- biotech experience • Knowledge, Skills and Abilities: Good leadership skills, effective at mentoring and training, and capable of motivating and integrating teams • Good planning and organizational skills to enable effective prioritization of workload • Solid interpersonal and problem-solving skills to enable working in a multicultural matrix organization • Capable of working effectively in a changing environment with sophisticated/ambiguous situations • Familiarity with the practices, processes, and requirements of clinical monitoring • Good judgment and decision-making skills • Effective oral and written communication skills, including English language proficiency • Capable of evaluating workload against project budget and adjusting resources accordingly • Sound financial acumen and knowledge of budgeting, forecasting and fiscal management • Strong attention to detail • Solid understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc. • Good digital literacy to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.
• Competitive remuneration • Annual incentive plan bonus • Healthcare • Range of employee benefits
Apply Now🔥 19 minutes ago
Senior Clinical Practice Manager responsible for provider performance and clinical quality oversight at MEDvidi. Ensuring telehealth compliance and operational execution in a regulated environment.
🔥 41 minutes ago
Regional Sales Manager driving growth of truck equipment and trailer business in Northeastern US. Interfacing with customers, developing forecasts, and enhancing profitability.
🔥 43 minutes ago
District Merchandise Manager responsible for sales optimization and category management at Floor & Decor. Collaborating with regional teams for product mix strategies across the Pacific Northwest and Rockies region.
🇺🇸 United States – Remote
💵 $140.4k - $217.6k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
🔥 58 minutes ago
Global Flagship Accounts Manager promoting customer satisfaction and revenue growth for a diverse technology innovator. Leading strategic relationships and account management initiatives for key customers.
🇺🇸 United States – Remote
💰 Post-IPO Equity on 2020-03
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
🔥 1 hour ago
Publisher Support Manager assisting Freestar's publishers with ad operations and troubleshooting issues on their websites. Collaborating with teams to optimize revenue generation.