384 matching jobs for “Clinical Study Specialist”

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Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.

Thermo Fisher Scientific

FSP Contract Specialist

Remote, Mexico +3 locations 4 postings

Join Us as a Site Contract Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 20, 2026

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Thermo Fisher Scientific

Site Contract Specialist

Ivry-sur-Seine, France

Join Us as a Site Contract Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Thermo Fisher Scientific

Participation Relations & Resolution Specialist

Austin, Texas, United States

Participation Relations & Resolution Specialist Are You... A critical thinker who asks questions, gathers facts, and considers multiple perspectives before …

Added Oct 16, 2026

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IQVIA Holdings

Data Entry Specialist

San Antonio, Texas, United States

Pay posted by employer$25,900–$64,800

… for performing all data entry functions as they relate to the completion of case report forms, by entering study data collected by the research team into the Electronic Data Capture (EDC) system. Data entry personnel …

Added Oct 16, 2026

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Thermo Fisher Scientific

(Sr) Clinical Research Associate - Client-dedicated (FSP) Netherlands

Remote, Netherlands

Join Us as a ( Senior) Clinical Research Associate in our client dedicated FSP team - Netherlands. Make an Impact at the Forefront of …

Added Oct 16, 2026

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Thermo Fisher Scientific

(Sr) Clinical Research Associate - Client-dedicated FSP - Belgium

Remote, Belgium

Join Us as a ( Senior) Clinical Research Associate in our client dedicated FSP team - Belgium – Make an Impact at the Forefront of …

Added Oct 16, 2026

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Thermo Fisher Scientific

Principal Country Approval Specialist

Remote, Poland

… taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research …

Added Oct 16, 2026

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Regeneron Pharmaceuticals

Sr. Specialist, Medical Coding

Hyderabad

Full time
Regular

… and commercializing medicines that change lives for people with serious diseases. We are seeking a Senior Specialist, Medical Coding to join our Clinical Data Management team. You will independently manage medical coding …

Added Oct 16, 2026

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Thermo Fisher Scientific

Country Approval Specialist - FSP

Remote, United Kingdom

Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Associate Contract Specialist

Remote, Argentina +2 locations 4 postings

Join Us as an Associate Site Contract Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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GE HealthCare Technologies

Senior Application Specialist

WuXi

… globally and generate design proposal. 2、 Evaluate, validate design by performing internal and external clinical studies. 3、 Has knowledge of best practices and how own area integrates with others; is aware of the …

Added Oct 27, 2026

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Abbott Laboratories

Sr Therapy Specialist

Korea - Seoul

… solutions for the treatment of structural heart disease. PRIMARY FUNCTION / OBJECTIVE: The Therapy Specialist (TS) has the responsibility (within a defined region of S. Korea) to meet the sales target and develop the …

Added Oct 23, 2026

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Thermo Fisher Scientific

Project Support Coordinator - Language Specialist

Bengaluru, India

Project Support Coordinator – Language Specialist Join Us and Make an Impact at the Forefront of Clinical Research Innovation We have successfully supported …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Country Approval Specialist

Remote, Romania

Join us as a Country Approval Specialist and make an impact at the forefront of innovation. We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Country Approval Specialist

Remote, Vietnam +6 locations 20 postings

Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 27, 2026

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Thermo Fisher Scientific

Country Approval Specialist - FSP

Austria, Austria +1 location 2 postings

Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Merck (MSD)

Associate Director, CDM Trial Lead, GDMS Clinical Data Management

COL - Cundinamarca - Bogotá (Colpatria) +2 locations

Under the direction of Therapeutic Area (TA) leadership, the CDM (Clinical Data Management) Trial Lead is accountable for end-to-end delivery of data management activities for …

Added Oct 16, 2026

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Thermo Fisher Scientific

Ctry Approval Specialist

Beijing, China

Added Oct 16, 2026

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Thermo Fisher Scientific

Associate Nutrition Specialist/Dietitian

Remote, Texas, USA

… or helping find cures for cancer. DESCRIPTION: Provides nutrition expertise and operational support for clinical trial nutrition programs and services. Supports the design, implementation, and delivery of …

Added Oct 16, 2026

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Thermo Fisher Scientific

Associate Nutrition Specialist / Dietitian

Remote, Texas, USA

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Contract Specialist

Remote, Mexico +3 more

Same role posted 4 times, once per location

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Site Contract Specialist – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to prepare and negotiate contracts, as well as finalize the contract process. As a Site Contract Specialist, you'll liaise and establish effective relationships with sites and internal functional teams. You will ensure quality, objectivity, and risk analysis in the efficient delivery of contracts.

What You’ll Do:
• Drafts, reviews, negotiates and finalizes agreements with study sites in accordance with local/accepted process.
• Negotiates within approved parameters both investigator grant budget negotiation parameters, contractual terms and conditions in accordance with company contractual considerations, client contractual considerations, established process with sites and follows established escalation routes.
• Ensures compliance to established negotiation parameters, authority approval, contractual process and client expectations.
• Ensures compliance of budgetary guidance, templates and process.
• Identifies and assesses legal, financial and operational risks and escalates to appropriate level of the organization per established processes.
• Provides recommendations and alternative resolutions to Investigator Contracts negotiations through established escalation channels.
• Coordinates with internal functional departments to ensure various site startup activities are aligned with contractual activities and mutually agreed upon timelines; ensures alignment of contract negotiation process for sites and study are properly aligned to the critical path for site activation.
• Achieve target cycle times for site activations.
• Ensures guidelines and processes are followed for efficient escalation of out of parameter issues as appropriate.

Education and 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 2-5 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 and Abilities:
• Good understanding of the principles of contract law, including a general understanding of laws that influence contract language, such as business, intellectual property and local tax and stamp laws
• Demonstrated ability to apply basic principles of investigator grant negotiation
• General understanding of business and financial principles that related to service agreements
• Effective communication skills (verbal & written) in English and local language
• Capable, with appropriate oversight, of drafting and negotiating contract provisions and budgetary issues within parameters
• Demonstrated ability in attention to detail
• Excellent analytical and decision based thinking skills
• Understanding of the pharmaceutical product development process and involvement of CROs
• Able to work independently or in a team environment
• Good organizational and time management skills
• Working knowledge of PPD SOP & WPDs
• Able to organize competing priorities logically and review outstanding contractual risk and issues
• Able to effectively use automated systems and computerized applications
• Ability to demonstrate a customer focused style of communication, problem solving and collaboration

Working Conditions and Environment:
• Ability to work in an upright and /or stationary position for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
• Frequent mobility required.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
• Frequently interacts with others to obtain or relate information to diverse groups.
• Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
• Regular and consistent attendance.

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