384 matching jobs for “Clinical Study Specialist”

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Thermo Fisher Scientific

FSP Site Contract Specialist

Remote, Poland

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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Abbott Laboratories

Manufacturing Specialist, Animal Care

United States - Illinois - Long Grove

Pay posted by employer$20.35–$40.65 per hour

Manufacturing Specialist, Animal Care Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself …

Added Oct 15, 2026

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IQVIA Holdings

Sr Site Activation Specialist

Madrid, Spain

Senior Site Activation Specialist Global Site Activation Spain Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 …

Added Oct 15, 2026

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Thermo Fisher Scientific

인재풀 - Country Approval Specialist (SSU)

Remote, Korea, Republic of

… Protection Act. This includes providing recruitment-related information and sending newsletters. Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical …

Added Oct 16, 2026

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GE HealthCare Technologies

Medical Director Clinical Development / Directeur(trice) médicale du développement clinique

Buc +1 location

Summary The Medical Director leads the clinical development strategy for assigned imaging products within Pharmaceutical Diagnostics (PDx). This role …

Added Oct 27, 2026

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Gilead Sciences

Supply Chain Specialist IV

Foster City, California, United States

Full time
Regular

Pay posted by employer$102,085–$132,110

The Supply Chain Specialist IV within Global Clinical Supply Chain (GCSC) Delivery team is responsible for supporting the execution and …

Added Oct 15, 2026

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Thermo Fisher Scientific

Country Approval Specialist - Client dedicated

Paris, France

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

FSP Country Approval Specialist II

Remote, Denmark

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

Country Approval Specialist - FSP - Portugal

Lisbon, Portugal

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 Bench Country Approval Specialist

Remote, Peru +2 locations 3 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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Bristol-Myers Squibb

Senior Specialist, Document Management

Warsaw-WeWork-PL

Full time
Regular

… email. To check your application status, please login to your Candidate Home Account. R1601850 : Senior Specialist, Document Management

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Country Approval Specialist (all level)

Remote, Singapore

Join Us as a Country Approval Specialist - Make an Impact at the Forefront of Innovation The Country Approval Specialist manages the preparation, …

Added Oct 16, 2026

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Thermo Fisher Scientific

Senior/Principal Drug Safety Specialist

Remote, Philippines

Join Us as a Senior/Principal Safety 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 Site Start Up Specialist

Budapest, Hungary

… site start up and communication with internal and external team members to ensure prompt site approval and study timelines are achieved. Support sites and study teams to achieve rapid site start up. ACCOUNTABILITIES Work …

Added Oct 16, 2026

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Regeneron Pharmaceuticals

Senior Research Specialist – TPK/PD

TARRYTOWN

Full time
Regular

Pay posted by employer$93,900–$153,300

… to develop life-changing medicines for people with serious diseases. We are seeking a Senior Research Specialist, TPK-PD to join our nonclinical analysis team supporting our Translational PK-PD organization. In this …

Added Oct 16, 2026

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Thermo Fisher Scientific

Trial Activation Approval Specialist III

Remote, Georgia

Join Us as a Senior Country Approval Specialist - Make an Impact at the Forefront of Innovation The Senior Country Approval Specialist manages the …

Added Oct 25, 2026

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Regeneron Pharmaceuticals

Sr. Specialist Data Quality & Insights

Hyderabad

Full time
Regular

… and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist - Data Quality & Insights to join our Data Management team in Hyderabad. In this hands-on role, you will …

Added Oct 18, 2026

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Thermo Fisher Scientific

Technical Sales Specialist – Proteomics

Gangnam-gu, Korea, Republic of

… and converting new sales opportunities across academic, government, pharmaceutical, biotechnology, and clinical research customers. Provide technical and scientific expertise throughout the sales cycle , including …

Added Oct 16, 2026

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Regeneron Pharmaceuticals

Senior Specialist – Data Lake Operations

Hyderabad

Full time
Regular

… and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist, Clinical Data Lake Operations to join our Data Management team, supporting our clinical data operations in …

Added Oct 22, 2026

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Thermo Fisher Scientific

Clinical Research Associate (Level I or II) - FSP - Paris, Lyon, Bordeaux

Remote, France

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Site Contract Specialist

Remote, Poland

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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 of independent contract and budget negotiation).
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 Polish 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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