58 matching jobs for “FSP CRA(Level II)”

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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 supported the top 50 pharmaceutical …

Added Oct 16, 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

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 …

Added Oct 15, 2026

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Thermo Fisher Scientific

CRA II/Sr CRA - Sponsor-Dedicated FSP - Germany (m/f/d)

Remote, Germany

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP CRA ─ with Sign-on Bonus

Remote, Korea, Republic of

Join Us as a Senior Clinical Research Associate (Level II) – 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 CRA I / CRA II - U.S. South Central Region - Multiple Therapeutic Areas

Remote, Texas, USA +4 locations

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

Added Oct 29, 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 supported the top 50 pharmaceutical …

Added Oct 25, 2026

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Thermo Fisher Scientific

CRA II/ Sr CRA I/ Sr CRA II - US Southeast Region - Multiple Therapeutic Areas Available

Remote, Florida, USA

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II

Remote, Vietnam

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II

Remote, North Carolina, USA 2 postings

CRA (Level II) Purpose: Performs and coordinates all aspects of the clinical monitoring and site management process. …

Added Oct 29, 2026

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Thermo Fisher Scientific

FSP Country Approval Specialist II

Remote, Denmark

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II

Remote, Mexico

Added Oct 16, 2026

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Thermo Fisher Scientific

Experienced Clinical Research Associate (CRA II/Sr CRA) - Montreal, QC Canada - Bilingual

Québec, Quebec, Canada

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Experienced CRA II/Sr CRA - US Northeast Region - Multiple Therapeutic Areas Available

Remote, Massachusetts, USA

Pay posted by employer$85,000–$135,000

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available

Chicago, Illinois, United States +5 locations

Pay posted by employer$66,800–$125,000

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Experienced Clinical Research Associate (CRA II/Sr CRA) - AR, KS, LA, MO, OK, TX - Multiple Therapeutic Areas Available

Remote, Texas, USA

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II - U.S. Northeast Region - Multiple Therapies

Pittsburgh, Pennsylvania, United States +5 locations

CRA (Level II) Purpose: Performs and coordinates all aspects of the clinical monitoring and site management process. …

Added Oct 30, 2026

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Thermo Fisher Scientific

Global Study Manager - FSP - EMEA

Remote, Bulgaria +2 locations

Added Oct 16, 2026

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Thermo Fisher Scientific

Global Study Manager - FSP - UK - PACT/MAP experience

Remote, United Kingdom

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA II/ Sr CRA I/ Sr CRA II - US Southeast Region - Multiple Therapeutic Areas Available

Remote, Florida, USA

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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 five 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.

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.

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 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.

Valid driver's license where applicable.

1-2 years of traveling on-site monitoring experience is required.

Therapeutic experience in at least one of the following areas: Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary.

Candidates must live within 60 miles of the nearest major airport. Up to 80% travel is expected.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, including a drug screening.

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

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