386 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

Senior CRA level II

Prague, Czechia

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA (Level I)

Bangkok, Thailand

The CRA Level I performs and coordinates different aspects of the clinical monitoring and site management process. The role conducts remote or on-site visits to assess protocol and …

Added Oct 16, 2026

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Thermo Fisher Scientific

Associate Project Manager Comparator

Allschwil, Switzerland

… projects, both internal and external. This is to ensure that the products are ready for the start of the study or as required by the customer. Timely preparation of reports and other information to customers is also …

Added Oct 22, 2026

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Thermo Fisher Scientific

Safety Reporting Coordinator

Hyderabad, India

… 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 27, 2026

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Thermo Fisher Scientific

Drug Safety Reporting Coordinator

Remote, Philippines

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr CRA

Remote, Mexico

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA I - Senior CRA (FSP)

Adelaide, Australia +1 location

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA I/ II- FSP - Spain

Madrid, Spain +1 location

… and building a long-term career? We are hiring both Junior and experienced CRAs who are passionate about clinical research and eager to work on innovative studies while being supported by a global organization committed …

Added Oct 16, 2026

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Bristol-Myers Squibb

Medical Science Liaison, Neurodegeneration (Southern California)

San Diego - CA - US

Full time
Regular

Pay posted by employer$166,090–$201,262

… also engage the top HCPs in high-disease burden hospitals. The MSL captures medical insights and acts as a clinical & scientific advisor to cross-functional partners. Ensures applicable interactions are aligned with …

Added Oct 15, 2026

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Bristol-Myers Squibb

Medical Science Liaison, Neurodegeneration (Michigan)

Ann Arbor - MI - US +1 location

Full time
Regular

Pay posted by employer$166,090–$201,262

Added Oct 15, 2026

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Thermo Fisher Scientific

QC Coordinator

Sofia, Bulgaria +5 locations

… status to maintain high satisfaction levels. Fostering strong connections with the internal Language Specialist Team and clinical study teams to promote customer delight. Ensuring accurate and consistent recording of QC …

Added Oct 16, 2026

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Johnson & Johnson

(Sr.) Medical Advisor, Hematology

Breda, The Netherlands

Full time
Regular

… sciences (with MD/PhD being an additional asset) Relevant experience within Medical Affairs and/or Clinical R&D in the pharmaceutical industry (preferably as MSL or MA) or equivalent significant experience in …

Added Oct 15, 2026

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Merck (MSD)

Medical Science Liaison Oncology

MEX - Federal District - Mexico City

… and up-to-date on all major studies, product information on our and other companies’ relevant therapies, clinical data and relevant pipeline data to provide the most balanced data to SLs, KDMs and the healthcare community …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA (Level II)

Shanghai, China +1 location 2 postings

Added Oct 27, 2026

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Thermo Fisher Scientific

FSP CRA (Level II)

Remote, China +1 location 10 postings

Added Oct 27, 2026

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Thermo Fisher Scientific

FSP CRA(Level II)

Remote, China +2 locations 10 postings

Added Oct 27, 2026

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Thermo Fisher Scientific

FSP CRA(Level)

Remote, China

Added Oct 21, 2026

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Thermo Fisher Scientific

CRA (Level II)

Beijing, China +2 locations 2 postings

Added Oct 16, 2026

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Thermo Fisher Scientific

Beijing CRA

Beijing, China

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP CRA (Level II)

Remote, China

Added Oct 16, 2026

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Thermo Fisher Scientific

Senior CRA level II

Prague, Czechia

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites and client company personnel. You may assist the project manager or clinical team manager on assigned projects and/or may assist in the mentoring and training of junior clinical team members. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:
• Monitors investigator sites with a risk-based monitoring approach, applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable
• Provides updates on potential trends noted across multiple sites and discusses potential strategies for their management to the Clinical Team Manager (CTM).
• Participates in investigator meetings as necessary. Identifies potential
• investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
• Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
• Contributes to the project team by mentoring new members, assisting in preparation of project publications/tools including informed consents, CRF guidelines and monitoring plans, and sharing ideas/suggestions with team members. Assists in project specific training for the clinical team where necessary. Identifies areas for potential process improvements & share potential solutions for improvements.
• Performs additional tasks as assigned by CTM or Clinical Manager of CRAs (CM-CRA) (e.g. trip report review, newsletter creation, lead CRA team calls etc).
• Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Perform QC check of reports generated from CTMS system where required.
• Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
• Responds to company, client and applicable regulatory requirements/audits/inspections federal regulatory requirements/audits.
• Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner

Education and Experience Requirements:
• Bachelor's degree in a life science related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years as a clinical research monitor).
• Valid driver's license where applicable.

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:
• Effective clinical monitoring skills
• Excellent understanding and demonstrated application of FDA guidelines, ICH GCPs, applicable regulations and procedural documents
• Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving.
• Manages Risk Based Monitoring concepts and processes
• Ability to mentor and train other monitors in a positive and effective manner
• Ability to evaluate medical research data and proficient knowledge of medical terminology
• Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
• Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
• Excellent interpersonal skills
• Strong attention to detail
• Effective organizational and time management skills
• Ability to remain flexible and adaptable in a wide range of scenarios
• Excellent team player with team building skills
• Ability to work independently as required
• Ability to utilize problem-solving techniques applicable to constantly changing environment
• Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
• Good English language and grammar skills
• Effective presentation skills
Working Conditions and Environment:
• Work is performed in an office/laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
• Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.
• May also include extended overnight stays.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions.
• Must be able to comply with specific sponsor/client/site requirements, even if not required by
• Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.

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