1,000+ matching jobs for “Clinical Research Associate”

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Thermo Fisher Scientific

Sr CRA (Level I and II)

Madrid, Madrid, Spain +1 location

… 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 Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP CRA II

Remote, Brazil

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA (Level II)

Remote, Argentina

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 level I

Remote, Argentina

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Senior CRA

Remote, South Africa

Join Us as a Senior Clinical Research Associate – 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 Sr CRA - Medical Device - East Coast

Remote, Indiana, USA

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

Added Oct 16, 2026

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IQVIA Holdings

CRA 2, Oncology, IQVIA Biotech

Durham, North Carolina, United States +6 locations

Pay posted by employer$74,500–$175,100

… initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. Collaborate with site staff to implement and track subject recruitment …

Added Oct 15, 2026

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IQVIA Holdings

Regulatory and Start Up Specialist - Poland

Warsaw, Poland

… Ethics Committee submissions Informed Consent Forms (ICFs) Investigator Pack (IP) release documentation Clinical Trial Agreements (CTAs) Support contract negotiation activities and timelines. Maintain accurate records …

Added Oct 15, 2026

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IQVIA Holdings

CRA 2, Single-Sponsor Dedicated

Amsterdam, The Netherlands

… clinical research expertise to drive meaningful outcomes for patients and sponsors around the world. As a Clinical Research Associate, you'll work across innovative studies and therapeutic areas, build your reputation with leading …

Added Oct 15, 2026

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Thermo Fisher Scientific

CRA (Level II)

Remote, India

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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Becton Dickinson

Senior Engineer – Applied ML/AI Algorithms R&D for Advanced Patient Monitoring

USA CA - Irvine Laguna Canyon

In person
Full time
Regular

Pay posted by employer$105,500–$168,800 USD

… enable earlier intervention, and drive better outcomes. This team operates at the intersection of research, product, and clinical translation. We partner closely with engineering, clinical, regulatory, and product …

Added Oct 27, 2026

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Amgen

Mgr Centralized Study Support

India - Hyderabad

Full time
Regular

… CSS roles within their team, ensuring they are positioned to deliver high-quality operational support to clinical programs and managing performance issues effectively and compassionately . Roles & Responsibilities: Team …

Added Oct 15, 2026

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IQVIA Holdings

Sr. CRA 1, IQVIA

Durham, North Carolina, United States +3 locations

Pay posted by employer$90,200–$175,100

… initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs …

Added Oct 15, 2026

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IQVIA Holdings

Experienced CRA - Single Sponsor Dedicated

Reading, United Kingdom

… and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, …

Added Oct 15, 2026

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IQVIA Holdings

Global Study Assoc. Director - Single Sponsor Dedicated

Buenos Aires, Argentina +3 locations

The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical …

Added Oct 15, 2026

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IQVIA Holdings

CRA II, Oncology

Manchester, United Kingdom

Added Oct 15, 2026

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IQVIA Holdings

Medical Director - Oncology , Sponsor Dedicated (Home-Based)

Warsaw, Poland

… Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and …

Added Oct 15, 2026

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Johnson & Johnson

Assoc II Stat Programmer

Chiyoda, Japan

Full time
Regular

Position Summary: The Associate Programmer is an individual contributor with basic knowledge of data structures, programming languages, and …

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 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Medical Director/Sr Medical Director - Pulmonary

Chapel Hill, North Carolina, United States

… with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and …

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr CRA (Level I and II)

Madrid, Madrid, Spain +1 more

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REQUIREMENTS · employer excerpt

Bachelor's degree in a life sciences 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 2+ 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.

About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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 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 Senior Clinical Research Associate (Level I), 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 rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF 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 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). Performs QC check of reports generated from CTMS system where required.
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 assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
Facilitates effective communication between investigative sites, the client company and the 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 other project work and initiatives for process improvement, as required.

REQUIREMENTS

Education and Experience Requirements:

Bachelor's degree in a life sciences 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 2+ 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
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application 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 manages Risk Based Monitoring concepts and processes
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 detailand the ability to perceive customers' underlying issues
Effective interpersonal skills
Strong attention to detail
Effective organizational and time management skills
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: proficient 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.
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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