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

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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 …

Added Oct 25, 2026

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IQVIA Holdings

Medical Director, Psychiatrist

Durham, North Carolina, United States

Pay posted by employer$115,900–$322,900

Job Level: Associate Medical Director, Psychiatrist Location: Home-based in the U.S J ob Overview Primarily acts as global and …

Added Oct 15, 2026

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Abbott Laboratories

Senior Scientist

United States > Madison : 501 Charmany Dr

Pay posted by employer$99,300–$198,700

… procedures on new assignments or projects. Working in a team setting, the Sr. Scientist will be involved in Research and Development projects serving as a technical lead and/or a subject matter expert in exploring and …

Added Oct 15, 2026

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Abbott Laboratories

Franchise Lead, Health Economics & Reimbursement (HE&R)(on-site)

Plymouth, Minnesota, United States +1 location

Pay posted by employer$129,300–$258,700

… Economics & Reimbursement professional to join our team on-site in Santa Clara, CA or Plymouth, MN . The Associate Director will be responsible for the proposals, development, and execution of value-focused economic and …

Added Oct 15, 2026

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Johnson & Johnson

Medical Director, Gastroenterology Therapeutic Area, US Medical Affairs

Horsham, Pennsylvania, United States of America

Full time
Regular

… Immunology organization. They will work closely with the other Gastroenterology Medical Directors (and Associate Directors) as well as partners in US and Global Medical Affairs, Real World Value and Evidence (RWV&E), …

Added Oct 15, 2026

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IQVIA Holdings

Specimen Mgmt Specialist

Koto-ku, Tokyo, Japan

Job Overview The Sr Specimen Management Associate is responsible for various activities associated with receipt, storage, and shipment of clinical …

Added Oct 15, 2026

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Amgen

Specialty/Senior Specialty Representative - Cardiovascular - Springfield, Il

Springfield, Illinois, United States

… each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our …

Added Oct 21, 2026

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Amgen

Specialty/Senior Specialty Representative - Cardiovascular - Springfield, Il

St. Louis, Missouri, United States

Full time
Regular

Added Oct 16, 2026

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Becton Dickinson

Sr. Medical Science Liaison

USA RI - Warwick +10 locations

Field
Full time
Regular

Pay posted by employer$149,600–$239,400 USD

… Align on medical strategy and key objectives with cross-functional partners, including medical, clinical, marketing, commercial, regulatory, R&D, and market access teams. Identify, segment, and map all relevant …

Added Oct 27, 2026

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Elevance Health

Nurse Appeals

Nashville, Tennessee, United States

Regular

… and summarizes medical information for medical directors, consultants and other external reviews. Research to determine appropriate medical necessity guidelines to apply for denied services. Utilizes guidelines and …

Added Oct 27, 2026

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Becton Dickinson

Group Product Marketer, Global Downstream

USA CA - Irvine Laguna Canyon

In person
Full time
Regular

Pay posted by employer$146,000–$233,600 USD

… Salesforce readiness (e.g., training on product, messaging, and competition) Define and build a body of clinical and economic evidence that supports the regional value proposition Manage budgets related to product line, …

Added Nov 4, 2026

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Zoetis

Laboratory Animal Behavior Intern

Lincoln

Full time
Regular

Role Description: Join a global animal welfare program that places behavioral medicine at the center of daily clinical care. This internship is designed for a PhD student in Behavioral Animal Science or DVM student with a …

Added Oct 15, 2026

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Zoetis

Laboratory Animal Veterinarian and Behavior Intern

Kalamazoo - Downtown Portage Street

Full time
Internship

Role Description: Join a global animal welfare program that places behavioral medicine at the center of daily clinical care. This internship is designed for a DVM graduate with a passion for the clinical application of …

Added Oct 15, 2026

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Danaher

Manufacturing Test Technician (Beam Test)

Nicholasville, Kentucky, United States

… 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 31, 2026

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Danaher

Precision Manufacturing Technician / Aperture Cleaning

Nicholasville, Kentucky, United States

Added Oct 31, 2026

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Danaher

Precision Manufacturing Technician

Nicholasville, Kentucky, United States

Added Oct 31, 2026

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Danaher

Quality Inspection Technician (Wafer Inspection)

Nicholasville, Kentucky, United States

Added Oct 31, 2026

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Thermo Fisher Scientific

CTM - SR CTM FSP

Remote, Peru

To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Client Procedural Documents, …

Added Oct 31, 2026

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Thermo Fisher Scientific

Medical Director / Senior Medical Director, Psychiatry

Remote, Mexico +5 locations

… Information Our detailed, goal-oriented Medical colleagues manage the safety profile of new drugs in clinical trials. As part of your work with beginning-to-end trial experience, you will expand your knowledge and …

Added Oct 16, 2026

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Thermo Fisher Scientific

Senior/Principal Drug Safety Specialist

Remote, Philippines

… 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 expert team, you’ll have the opportunity …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA II in Romania

Remote, Romania

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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 performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring 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. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix.

Major Job 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 (CTMS)).

• 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.

• Travel requirement >75%.

Qualifications: Education and Experience:

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 1 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:

• 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

Management Role:

No management responsibility.

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

Physical Requirements:

• Ability to work in an upright and /or stationary position for 6-8 hours per day

• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists

• Frequent mobility required.

• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck

• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer

• Ability to access and use a variety of computer software developed both in-house and off the-shelf

• Ability to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and

sentences

• Frequently interacts with others to obtain or relate information to diverse groups

• Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence

• Ability to perform under stress

• Ability to multi-task

• Regular and consistent attendance

Percent Billable:

80% - 100%

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