367 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.
TFS
Thermo Fisher Scientific
Remote, Costa Rica
Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …
Added Oct 16, 2026
Foster City, California, United States
Pay posted by employer $117,895–$152,570
The Senior Supply Chain Specialist , Clinical Logistics plays a critical role in supporting global clinical development programs by ensuring …
Added Oct 15, 2026
Durham, North Carolina, United States +1 location
Pay posted by employer $74,600–$216,000
… Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to …
Added Oct 15, 2026
Buenos Aires, Argentina
Clinical Files Specialist - Entry Level role Work modality: Hybrid Job Overview Perform daily administrative …
Added Oct 15, 2026
Denver, Colorado, United States
Johnson & Johnson is hiring for a Field Clinical Specialist for Shockwave Medical Inc. located in Colorado / Wyoming . At Johnson & Johnson, we believe …
Added Oct 15, 2026
TFS
Thermo Fisher Scientific
Remote, Mexico +2 locations
Join Us as a FSP Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …
Added Oct 16, 2026
TFS
Thermo Fisher Scientific
Remote, New York, USA
Pay posted by employer $76,700–$95,000
… and autoimmune diseases by providing healthcare professionals with advanced diagnostics technologies and clinical expertise. Our key businesses: allergy, autoimmunity, and systems. Location: This is a field sales position …
Added Oct 16, 2026
Cambridge, Massachusetts, United States +1 location
Pay posted by employer $89,000–$116,000
Every clinical trial depends on investigational medicine arriving at the right place, at the right time, and in the right …
Added Oct 16, 2026
TFS
Thermo Fisher Scientific
Sofia, Bulgaria
As part of our PPD clinical research team, you’ll have the opportunity to support groundbreaking studies that make a real difference in …
Added Oct 16, 2026
TFS
Thermo Fisher Scientific
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, our …
Added Oct 20, 2026
Lafayette, Louisiana, United States +1 location
Job Description Johnson & Johnson is hiring for a Field Clinical Specialist for Shockwave Medical Inc. located in the Lafayette/Lake Charles, LA area. At Johnson & Johnson, …
Added Oct 15, 2026
USA - Pennsylvania - West Point +1 location
Pay posted by employer $117,000–$184,200
The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain …
Added Oct 16, 2026
Salt Lake City, Utah, United States
Johnson & Johnson is hiring for a Field Clinical Specialist – Circulatory Restoration to join our team located in the Rockies Region (Salt Lake City, UT). …
Added Oct 15, 2026
Atlanta, Georgia, United States
Pay posted by employer $61,300–$122,700
… to patient tracing when required. Manage physical inventory within the assigned territory. Collect and study information about new and existing products, monitoring competitor sales, prices, and products. Analyze …
Added Oct 15, 2026
Houston, Texas, United States
Pay posted by employer $79,000–$126,500
Job Description Johnson & Johnson is hiring for a Field Clinical Specialist for Shockwave Medical Inc. located in Houston, TX. You must currently reside in the area. We do …
Added Oct 15, 2026
USA - Pennsylvania - West Point +1 location
Pay posted by employer $117,000–$184,200
The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain …
Added Oct 16, 2026
Frankfurt, Hesse, Germany
include operational delivery of strategic clinical studies assigned to the country, in accordance with ICH/GCP, Incyte SOPs, local operating guidelines and …
Added Oct 15, 2026
Taipei, Taiwan
The Senior Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned …
Added Oct 16, 2026
TFS
Thermo Fisher Scientific
Remote, Israel
Join Us as a Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top …
Added Oct 16, 2026
Las Vegas, Nevada, United States
Pay posted by employer $79,000–$126,500
Job Description Johnson & Johnson is hiring for a Field Clinical Specialist for Shockwave Medical Inc. located in the Las Vegas, NV. You must currently reside in the area. …
Added Oct 15, 2026
Frankfurt, Hesse, Germany
Required Skills and Qualifications · employer excerpt At least 5 years’ clinical research experience as CRA or Lead CRA or Project Manager. Bachelor or higher University degree in life sciences, nursing or medical background preferred. Proven experience in feasibility and study start-up. Fluency in German and English language Demonstrated knowledge of clinical trial methodology and drug development process, related to monitoring clinical trials, GCP, SOP and country-specific regulatory requirements. 4 more in the full description below.
About this opportunity Original employer description The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients.
The country Clinical Research Lead (CRL) responsibilities include operational delivery of strategic clinical studies assigned to the country, in accordance with ICH/GCP, Incyte SOPs, local operating guidelines and local requirements. The Clinical Research Lead works locally to ensure country goals for recruitment and completion of key R&D sponsor deliverables are met.
Main Responsibilities
Oversee local CRO activities, acting as Single Point of Contact for key and strategic outsourced clinical studies, to ensure corporate and country objectives are reached and potential country issues properly followed-up. Collaborate and liaise with Clinical Study Teams and Global Monitoring, for Sponsor’s clinical studies conducted within country, ensuring key project milestones and high quality are delivered. Partner with local Study Startup Specialist or Clinical Research Associates to ensure consistency and accuracy of all core documents for local EC submission (i.e. submission pack, document customization, translations, quality check). Act as the central point of contact for feasibilities in the country, for clinical studies when feasibilities are requested or deferred to country by Global Teams. Carry out top Level feasibilities, to collect key information on competitive clinical studies, marketed and non-marketed drugs, regulatory concerns, Standard of care, etc Build up professional relationship with the investigators and Key Opinion Leaders. Support the Global Monitoring team to conduct co-monitoring and CRA assessment visits, when needed and requested. Act as a Site Relationship Partner for specific studies, to build and retain relationships through the lifecycle of the clinical study, to ensure an effective clinical study conduction and completion. Act in accordance with company policies and procedures, SOPs, ICH/GCP guidelines, FDA regulations and local regulatory bodies. Collaborates and interact with Medical Affairs Department, QA, Global Monitoring, clinical Study Start-Up teams, Global Clinical Trial Managers (CTMs), Global Regulatory and other as work needs.
Required Skills and Qualifications
At least 5 years’ clinical research experience as CRA or Lead CRA or Project Manager. Bachelor or higher University degree in life sciences, nursing or medical background preferred. Proven experience in feasibility and study start-up. Fluency in German and English language Demonstrated knowledge of clinical trial methodology and drug development process, related to monitoring clinical trials, GCP, SOP and country-specific regulatory requirements. Strong attitude to problem solving, effectively prioritize tasks and working independently. Effective organizational and time management skills. Ability to establish and maintain effective working relationships with co-workers, managers, internal and external stakeholders. Available for domestic and international travel, including overnight stays up to approximately 20% of the working week.
Please apply with your English CV.
Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Why this result? · Employer labels Keywords also found in description