Bogota, Capital District, RAP (Especial) Central, Colombia · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Sr Clinical Trial Manager - Make an Impact at the Forefront of Innovation The Clinical Trial Manager is accountable for achiev…
Skills: Clinical Trial Management, ICH GCP, Clinical Monitoring, Trial Master File Management, Budgeting and Forecasting
Richmond, Virginia, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Fluctuating Temps hot/cold, Laboratory Setting, Lou…
Skills: Laboratory Instrumentation, Microsoft Excel, Microsoft Word, Hamilton Venus, TECAN EVOware
Bengaluru, Karnataka, India · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Job Description Are you passionate about making a positive impact on the world? Thermo Fisher Scientific Inc. is currently seeking a highly…
Skills: Hazard Communication, Chemical Hazard Assessment, SDS Authoring, GHS Compliance, Regulatory Affairs
Richmond, Virginia, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Loud Noises (Equipment/Machiner…
Skills: Refrigeration, CFC Certification, HVAC, Plumbing, Electrical
Hillsboro, Oregon, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As a Senior Financial Analyst, you play a critical role in supporting the operations business at the Hillsboro site for the Electron Micros…
Skills: Financial Forecasting, Budgeting, Variance Analysis, Production Cost Analysis, Inventory Optimization
Los Angeles, California, United States · On-site
$26/hr–$42/hr
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our coll…
Skills: Calendar Management, Travel Coordination, Executive Support, Microsoft Office Suite, Internal Communications
Bengaluru, Karnataka, India · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our coll…
Skills: Technical Sales, UPLC-MSMS, Triple Quad, HRMS, Market Development
Bengaluru, Karnataka, India · Remote OK
Work Schedule Other Environmental Conditions Office Job Description Summarized Purpose: We are looking for a Lead Full-Stack AI Engineer with strong frontend expertise to design and deliver production AI web applications…
Skills: React/Next.js, TypeScript, Python, FastAPI, LLM APIs
São Paulo, São Paulo, Brazil · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported th…
Skills: Clinical Monitoring, ICH-GCP, Risk-Based Monitoring, Root Cause Analysis, Site Management
São Paulo, São Paulo, Brazil · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top …
Skills: Clinical Monitoring, ICH-GCP, Risk-Based Monitoring, Root Cause Analysis, Site Management
Birmingham, England, United Kingdom · Hybrid
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, our Finance teams are important to our business and functional teams to make educated, sound decisions that dr…
Skills: Management Accounting, Financial Reporting, Variance Analysis, Business Partnering, Budgeting
Orlando, Florida, United States · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Job Description About Us: Here at Thermo Fisher Scientific, our industry-leading scale means unparalleled commercial reach, uni…
Skills: Medical Sales, B2B Technical Sales, CRM, Salesforce.com, Account Planning
Perth, Scotland, United Kingdom · On-site
Work Schedule Rotational shift days Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Labo…
Skills: Microbiology, Quality Control, Growth Promotion Testing, Fertility Testing, Antibiotic Sensitivity Testing
Franklin, Massachusetts, United States · On-site
$21/hr–$23/hr
Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Fluctua…
Skills: Inventory Management, Data Entry, Sample Tracking, Material Handling Equipment, Good Manufacturing Practices
Bengaluru, Karnataka, India · Hybrid
Work Schedule Second Shift (Afternoons) Environmental Conditions Office Job Description Join Us as a CDM Programmer II – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceuti…
Skills: SAS, SQL, Crystal Reports, JReview, Relational Database Systems
Bengaluru, Karnataka, India · Remote OK
Work Schedule Other Environmental Conditions Office Job Description Summarized Purpose: We are seeking a Sr. Report Developer with strong Tableau expertise to design, develop, administer, and support enterprise reporting…
Skills: Tableau Report Development, Tableau Server Administration, Advanced SQL, Data Modeling, AWS Integration
Singapore, Singapore · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our coll…
Skills: Quality Assurance, GMP Compliance, ISO 13485, Cold Chain Logistics, Root Cause Analysis
Taguig, Metro Manila, Philippines · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description This role is part of the global Site Payments team. As a Site Payment Associate (Funds Management), you will be dealing with one of the mos…
Skills: Funds Management, Billing Calculation, Financial Tracking, Clinical Trial Payments, MS Excel
Ciudad de México, Mexico · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join us as Project Manager Clinical Supplies - To manage the end-to-end supply chain for clinical trials, ensure timely and efficient distr…
Skills: Clinical Supply Chain Management, Project Management, GxP Compliance, Inventory Management, Stakeholder Management
Middleton, Wisconsin, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our coll…
Skills: Systems Administration, Windows Server, Linux, Relational Database Concepts, MS Office
Bogota, Capital District, RAP (Especial) Central, Colombia • Remote OK
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
The Clinical Trial Manager is responsible for achieving final clinical deliverables and clean data within contractual timelines and budgets. This includes managing operational and quality aspects of studies, developing clinical tools, and coordinating with cross-functional teams to ensure compliance with ICH GCP.
Candidates must hold a bachelor's degree or equivalent with at least 5 years of relevant experience in clinical trial management. Required skills include strong leadership, financial acumen, and a deep understanding of FDA and ICH/GCP regulations.
Join Us as a Sr Clinical Trial Manager - Make an Impact at the Forefront of Innovation
The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. The Clinical Trial Manager interprets data on project issues and makes good business decisions with support from experienced team members or line manager. Works to ensure that all clinical deliverables meet the customer's time/quality/cost expectations. Maintains profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team. The position involves working on projects of low to moderate complexity and as part of a team of CTMs.
The therapeutic scope includes Cardiovascular & Internal Medicine- Nephrology, Dermatology, GI, (UC/CD, EOE, EE), Cardiovascular, Liver, Immunology, Rare Disease, Diabetes, Obesity, Dyslipidemia, Women's Health, Rheumatology, (RA, SLE, Gout), Cell and Gene Therapy, CAR-T in Autoimmune.
Nephrology: (CKD, Delayed Graft Function, Antibody-Mediated Rejection, IgA Nephropathy, Lupus Nephritis)
Dermatology: Atopic Dermatitis, Psoriasis, Hidradenitis Suppurativa (HS), Prurigo Nodularis, Rosacea, Vitiligo, Alopecia Areata
What You'll Do:
• Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
• Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
• Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and lead 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.
• Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution. Continuously monitor or co-monitors clinical trials to assess performance and ensure contractual obligations are met. In smaller regions, may routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
• May communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
• May coordinate all start-up activities and ensures that timely ethics committee and regulatory submissions (if appropriate) are addressed. Ensure that essential document quality meets the expectation of Regulatory Compliance Review. Review and follows up on all questions raised by the ethics committees.
• May provide input into preparation of forecast estimates for clinical activities. Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.
Education & Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, 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 complex/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 acument 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 computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.
Working Conditions and Environment:
• Work is performed in an office environment with exposure to electrical office equipment.
• Frequently drives to site locations and frequently travels both domestic and international.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $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. For more information, please visit www.thermofisher.com.
Offices: 168 Third Avenue, Waltham, MA, US
About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $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. For more information, please visit www.thermofisher.com.
Offices: 168 Third Avenue, Waltham, MA, US
