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

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Thermo Fisher Scientific

CRA (Level II)

Kyiv, Ukraine

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation! We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA (Level Ⅱ）

Beijing, China

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

… Manages procedures and guidelines from different sponsors and/or supervising environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance …

Added Oct 27, 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

FSP Sr CRA (Level I)

Shanghai, China

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA (Level I or II) FSP - Athens

Remote, Greece

… 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 …

Added Oct 22, 2026

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Thermo Fisher Scientific

CRA II for FSP

Remote, Mexico

Join Us as a Clinical Research Associate (Level II) for FSP– Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA II / Sr CRA - FSP - Austria

Vienna, Austria

Join Us as a Clinical Research Associate (Level II) / Sr CRA – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA I / CRA II FSP Denmark

Remote, Denmark

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Senior CRA level II

Prague, Czechia

… 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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

SR CRA (Level II)

Remote, Argentina

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA Level II/Senior CRA (Thessaloniki/Athens)

Remote, Greece

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation As part of our global team, you’ll have the opportunity …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP CRA I or II

Remote, Texas, USA

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

Added Oct 28, 2026

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Thermo Fisher Scientific

CRA I/II/ Sr CRA - FSP - UK

Remote, United Kingdom

… customers manage capacity and set programs up for success. Discover Impactful Work: Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP CRA I & CRA II - Respiratory & Cardiovascular - Southeast region

Remote, Florida, USA

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

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr CRA (Level I and II)

Madrid, Spain +1 location

Locations considered: Madrid (Hybrid basis) Barcelona (remote basis) Position: Sr CRA (Level I and II) Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the …

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr CRA I/II - FSP - Norway

Remote, Norway

Join Us as a Senior Clinical Research Associate (Level I) – 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

CRA - FSP - Denmark

Remote, Denmark

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr CRA I/II - FSP - Spain

Remote, Spain

Join Us as a Senior Clinical Research Associate (Level I) – 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

CRA Levels II/Sr - FSP - Portugal

Remote, Portugal

… 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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA (Level II)

Kyiv, Ukraine

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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.

Position Overview:
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.

Main Duties & Responsibilities:

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.

Required Education and Experience:

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.

Required 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-depth investigation 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 flexible 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

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. 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.

Apply today to help us deliver tomorrow’s breakthroughs!

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