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

How results work

Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.

Thermo Fisher Scientific

Sr CRA (Level I) - FSP

Remote, Colombia

Descripción de puesto 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 28, 2026

Save job

Danaher

Senior Cybersecurity GRC Analyst (3 -4 years)

Bengaluru, Karnataka, India

Regular

… 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

Save job

Amgen

Manager 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

Save job

Thermo Fisher Scientific

Assistant CRA

Remote, Turkey

Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation! We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

Save job

Elevance Health

Advanced Analytics Consultant

Indianapolis, Indiana, United States +2 locations

Full time
Regular

… on test/pilot outcomes. Develops targeting criteria or customer segmentation based on analytical insights, clinical inputs, product design and operations considerations; develops predictive models and other tools that help …

Added Oct 27, 2026

Save job

Amgen

Sr Manager Centralized Study Support (CSS)

India - Hyderabad

… Study Support (CSS). This role ensures delivery of high‑quality centralized operational support across clinical programs and alignment of resources with organizational priorities. Roles & Responsibilities: Team …

Added Nov 5, 2026

Save job

Thermo Fisher Scientific

Operations Strategy Consultant

Remote, China +1 location

… 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

Save job

Danaher

Senior Human Factors Engineer

Bengaluru, Karnataka, India

Regular

Added Oct 15, 2026

Save job

Danaher

Senior Human Factors Engineer

Bengaluru, Karnataka, India

Regular

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

FSP CRA People Manager

Remote, Mexico +1 location

Join Us as an Associate Manager Clinical Operations – Make an Impact at the Forefront of Innovation We have successfully supported …

Added Oct 18, 2026

Save job

IQVIA Holdings

Global Study Manager - Single Sponsor dedicated (in EMEA)

Warsaw, Poland +2 locations

… GSAD with budget management, such as external service provider invoice reconciliation. • Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international …

Added Oct 15, 2026

Save job

IQVIA Holdings

资深咨询总监 Principal, cbh & iHEALTH

Shanghai, China

… 8.Proficient in Mandarin and English (in both verbal and written). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare …

Added Oct 15, 2026

Save job

Danaher

Development Scientist I

Chaska, Minnesota, United States

Regular

Pay posted by employer$32.00–$34.25 per hour

Added Oct 21, 2026

Save job

Amgen

Precision Medicine Global Biomarker Lead

United States - Remote

… cancer. 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 Nov 5, 2026

Save job

Amgen

Lab Operations Manager

United States - Remote

Full time
Regular

… conditions. 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 15, 2026

Save job

Thermo Fisher Scientific

Assistant CRA

Athens, Attica, Greece

Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation! We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

Save job

Thermo Fisher Scientific

CRA (Level II) - FSP

Remote, Peru +1 location 4 postings

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active …

Added Oct 16, 2026

Save job

Thermo Fisher Scientific

CRA (Level I) - FSP

Remote, Chile

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active …

Added Oct 16, 2026

Save job

IQVIA Holdings

Analyst - Assoc Consultant, Real World Solutions (Epidemiologist)

Taipei, Taiwan +2 locations

… and generation of evidence around key epidemiological features for real world studies Perform desk research, literature reviews and data analysis Work closely with various project team members including project …

Added Oct 15, 2026

Save job

Amgen

Sr Mgr Centralized Study Support

India - Hyderabad

Full time
Regular

… Study Support (CSS). This role ensures delivery of high ‑ quality centralized operational support across clinical programs and alignment of resources with organizational priorities. Roles & Responsibilities: Team …

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

Sr CRA (Level I) - FSP

Remote, Colombia

View job

Save job

About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Descripción de puesto

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 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 other project work and initiatives for process improvement, as required.

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, including:
– A minimum of 3 years of completed on-site clinical monitoring experience.
– Experience in infectious disease (pneumonia) and ophthalmology clinical studies is preferred.

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:
• 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.

Why this result? · Employer labels

Keywords also found in description

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.