384 matching jobs for “Clinical Study Specialist”

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Thermo Fisher Scientific

FSP CRA II (Neuro & Rare Disease) - US West

Remote, California, USA

Pay posted by employer$57,100–$87,125

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

Added Oct 15, 2026

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Pfizer

[MA] Senior Medical Affairs Scientist Manager - Amyloidosis (Cardiology)

Tokyo, Japan

Full time
Regular

… establish Pfizer as a trusted scientific partner in the evolving amyloidosis treatment landscape, bridging clinical insights with Medical Affairs excellence. • Focus on designated products through a team of MAS. • Lead …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA II in Romania

Remote, Romania

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

Added Oct 25, 2026

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Bristol-Myers Squibb

Manager, Medical Science Liaison, Cardiovascular

Otemachi-JP

Full time
Regular

contributes to the generation of medical insights related to disease areas, clinical practice, and evolving treatment landscapes. From pre‑launch through post‑launch phases, this position …

Added Oct 15, 2026

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Johnson & Johnson

[HCC] Senior Manager, Health Care Compliance, Innovative Medicine R&D – Japan & Korea

Chiyoda, Japan

Full time
Regular

… independent and risk-based leadership that enables ethical, patient-centric and compliant execution of clinical development, External Scientific Innovation and related scientific activities. Working across two distinct …

Added Oct 15, 2026

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Johnson & Johnson

MSL Neurociencias - Barcelona

Barcelona, Spain

Full time
Regular

… abreast of medical and scientific knowledge. Continuous update on products, patient’s treatment trends, clinical activities and studies conducted within the therapeutic area in their region. Development and maintenance …

Added Oct 15, 2026

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Johnson & Johnson

MSL Oncología - Málaga

Málaga, Spain +1 location

Full time
Regular

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior Scientist - Chromatography & LCMS

Richmond, Virginia, United States

Pay posted by employer$72,000–$120,000

… 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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IQVIA Holdings

Contracts Analyst 1

Sofia, Bulgaria +2 locations

… while developing knowledge of contract management practices within the CRO environment. The Contract Specialist I works closely with internal project teams and customers and supports senior team members on more complex …

Added Oct 15, 2026

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IQVIA Holdings

Associate Director, Client Services - IQVIA Medical Communications

Reading, United Kingdom +1 location

… of Practice to identify opportunities to cross sell solutions and extend relationships with clients from clinical study support into Medical Affairs Communications Accountable for ensuring accurate forecasting, invoicing, …

Added Oct 15, 2026

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Merck (MSD)

Principal Scientist (Director), Translational Medicine - Infectious Diseases

USA - California - South San Francisco (Grand Ave) +3 locations

Pay posted by employer$260,300–$409,700

We have an exciting opportunity for a physician-scientist to join our group as a Principal Scientist (Clinical Director) in Translational Medicine/Early Clinical Development in the Infectious Diseases Therapeutic Area …

Added Oct 19, 2026

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Regeneron Pharmaceuticals

Associate Director, External Data Acquisition and Delivery

Cambridge +3 locations

Full time
Regular

Pay posted by employer$154,800–$252,800

… life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Data Management team. As an Associate Director, External Data Acquisition and Delivery (EDAD), you will …

Added Oct 16, 2026

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IQVIA Holdings

Global Value Dossiers Writer - Global Health Economics team - Athens

Athens, Greece

The team & the company IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects …

Added Oct 15, 2026

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IQVIA Holdings

Global Value Dossiers Consultant - Global Health Economics team - UK

London, United Kingdom

Added Oct 15, 2026

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Johnson & Johnson

[Innovative Medicine] メディカルアフェアーズ本部ヘマトロジー部門ヘマトロジー部ヘマトロジーメディカルサイエンスリエゾン

Chiyoda, Japan

Full time
Regular

… needs for medical advancement in their therapeutic area and optimizing the value of Janssen products. Specialist (in addition to above;) • Has the responsibility to lead the projects/tasks of the MSL group in their …

Added Oct 15, 2026

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Johnson & Johnson

[Innovative Medicine]メディカルアフェアーズ本部イムノロジー部門イムノロジー部イムノロジーメディカルサイエンスリエゾングループメディカルサイエンスリエゾン

Chiyoda, Japan

Full time
Regular

Added Oct 15, 2026

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Johnson & Johnson

[Innovative Medicine] メディカルアフェアーズ本部ヘマトロジー部門ヘマトロジー部 AMLメディカルサイエンスリエゾン

Chiyoda, Japan +1 location

Full time
Regular

… needs to support medical advancement in the therapeutic area and maximize the value of J&J products. Specialist Level In addition to the responsibilities above: Lead projects and key initiatives within the MSL group in …

Added Oct 16, 2026

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Danaher

Staff Medical & Scientific Affairs Liaison - Infectious Diseases and Microbiology

Austin, Texas, United States

Regular

Pay posted by employer$135,000–$150,000 per year

… improvement, you help turn ideas into impact – innovating at the speed of life. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory’s …

Added Oct 15, 2026

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Johnson & Johnson

[Innovative Medicine] メディカルアフェアーズ本部イムノロジー部門イムノロジー部イムノロジーメディカルサイエンスリエゾングループメディカルサイエンスリエゾン (IBD)

Chiyoda, Japan +1 location

Full time
Regular

Added Oct 16, 2026

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Johnson & Johnson

[Innovative Medicine] メディカルアフェアーズ本部イムノロジー･肺高血圧症･ニポカリマブ部門ポートフォリオ部ポートフォリオメディカルサイエンスリエゾングループメディカルサイエンスリエゾン

Chiyoda, Japan

Full time
Regular

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP CRA II (Neuro & Rare Disease) - US West

Remote, California, USA

Pay posted by employer$57,100–$87,125

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate (Level II) – 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 perform and coordinate all aspects of the clinical monitoring and site management process. As a 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. 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.
• 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. Performs 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.
• 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).
• 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.
• Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
• Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
• Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:
• Bachelor's degree in a life sciences related fieldor 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 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
• 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:
• Proven clinical monitoring skills
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
• Well-developed critical thinking skills, including but not limited to: critical mindset, in-depthinvestigation for appropriate root cause analysis and problem solving
• Ability to manage Risk Based Monitoring concepts and processes
• Good 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
• Good organizational and time management skills
• Effective interpersonal skills
• Attention to detail
• Ability to remain flexibile and adaptable in a wide range of scenarios
• Ability to work in a team or independently as required
• Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
• Good English language and grammar skills
• Good 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

Compensation and Benefits

The salary range estimated for this position based in California is $57,100.00–$87,125.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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