384 matching jobs for “Clinical Study Specialist”

How results work

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

Sr Site Contract Specialist

Warsaw, Poland

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

Added Oct 16, 2026

Save job

Labcorp Holdings

Data Specialist III

Bengaluru, India

1.Engage client data management during start up. • Create protocol folder(s) for study documentation. • Add entries into individual protocol spreadsheet. • Review Statement of Work (SOW) for …

Added Oct 20, 2026

Save job

IQVIA Holdings

Senior Site Activation Specialist - Belgium

Charleroi, Belgium +6 locations

We are looking for a Freelance Senior Site Activation Specialist based in Belgium to support country-level clinical trial start-up and site management activities. This role …

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

Principal Regulatory Affairs Specialist

São Paulo, Brazil

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

Added Oct 27, 2026

Save job

IQVIA Holdings

… Data Management team leaders to report on the quality of data collection and tasks done. • Attend internal study meetings and internal/ sponsor audits. • Assist in tracking and managing the projects, oversee project …

Added Oct 15, 2026

Save job

IQVIA Holdings

Sr Site Activation Specialist

Prague, Czech Republic

Senior Site Activation Specialist Global Site Activation Czech Republic, Hybrid Make an impact on patient health! IQVIA’s Global Site …

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

Country Approval Specialist/ Sr. Country Approval Specialist - FSP client dedicated

Sofia, Bulgaria +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

Save job

IQVIA Holdings

Senior/ Site Activation Specialist

Kuala Lumpur, Malaysia

Perform feasibility, site identification, site contract negotiation, and other study start-up activities, as assigned. Distribute and collect CDAs for potential study sites. Provide …

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

Senior Country Approval Specialist

Remote, North Carolina, USA

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 16, 2026

Save job

Thermo Fisher Scientific

Import & Export Operations Specialist

Taipei, Taiwan

… Join our team at Thermo Fisher Scientific where you'll contribute to managing logistics operations for clinical trials, pharmaceutical products, and scientific equipment. As a Logistics Specialist I, you'll coordinate …

Added Oct 16, 2026

Save job

Thermo Fisher Scientific

Associate Country Approval Specialist

Bellshill, United Kingdom

… 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 …

Added Oct 16, 2026

Save job

IQVIA Holdings

Specimen Mgmt Specialist

Koto-ku, Tokyo, Japan

… Associate is responsible for various activities associated with receipt, storage, and shipment of clinical specimens. Responsible for equipment maintenance. Guides entry level staff on routine procedures. …

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

FSP Clinical Research Associate I - Bilingual French QC Canada

Remote, Canada

Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top …

Added Oct 27, 2026

Save job

Thermo Fisher Scientific

Clinical Research Associate II (CRA II) – FSP Business Unit

Remote, Romania

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

Added Oct 16, 2026

Save job

Abbott Laboratories

Therapy Specialist, TAVI Franchise EAST

Shinjuku, Japan

Job Purpose and Scope Clinical Therapy Specialists provide technical, clinical, educational and sales support to ensure safe adoption and …

Added Oct 15, 2026

Save job

IQVIA Holdings

Site Activation Specialist, ICF Lead

Buenos Aires, Argentina

… quality standards, and agreed project timelines Perform feasibility assessments, site identification, study start-up, and site activation activities in line with regional regulatory requirements Prepare, review, and …

Added Oct 15, 2026

Save job

IQVIA Holdings

Sr Site ID & Feasibility Specialist

Istanbul, Turkey

Sr Site ID & Feasibility Specialist Turkey - Hybrid Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, …

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

FSP Bench Contract Specialist

Vietnam, Vietnam +2 locations 3 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 27, 2026

Save job

Thermo Fisher Scientific

Contract Specialist - FSP - Spain

Madrid, Spain

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

Save job

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

Save job

Thermo Fisher Scientific

Sr Site Contract Specialist

Warsaw, Poland

View job

Save job

About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Sr 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

Why to join us

At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development program, ensuring you reach your potential.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Our 4i Values:

Integrity – Innovation – Intensity – Involvement

If you resonate with our 4i values above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, submit your application – we’d love to hear from you!

Apply today to help us deliver tomorrow’s breakthrough.

Why this result? · Employer labels

Keywords also found in description

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.