713 matching jobs for “Senior 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

CRA II / Sr CRA - FSP - Austria

Vienna, Vienna, Austria

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

Added Oct 16, 2026

Save job

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

Save job

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

Save job

IQVIA Holdings

Associate Group Leader / In Vivo Unit Manager

Portishead, United Kingdom

offers the opportunity to play a key part in high-quality research, supporting ethically conducted science and leading a committed animal care team. Main Tasks Operational: …

Added Oct 15, 2026

Save job

IQVIA Holdings

Director/Senior Director, Business Development, Biotech

London, United Kingdom +8 locations

… european Biotech market, and therefore we are seeking an ambitious individual with a proven track record in clinical sales. The role will be responsible for increasing our client portfolio, and therefore be required to sell …

Added Oct 15, 2026

Save job

Amgen

Quality Compliance Senior Manager

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 Oct 21, 2026

Save job

Johnson & Johnson

Senior Supervisor (Team Lead) Biologics AD

Ringaskiddy, Cork, Ireland

Full time
Regular

Position Title: Senior Supervisor (Team Lead) Biologics AD Cork Department: TDS-AD Cork Report to: Associate Director/Senior …

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

Medical Director/Senior Medical Director - Rheumatology/Dermatology

Remote, Argentina +1 location

Join Us as an Medical Director/Senior Medical Director – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll …

Added Oct 16, 2026

Save job

Merck (MSD)

Sr.Manager, Project Management

Beijing, Beijing, China

… departments, divisions, and franchises, including preparation of background documents and presentations to senior management. Effective execution of management-approved strategic plans for assigned projects; this includes …

Added Oct 16, 2026

Save job

Thermo Fisher Scientific

Senior/Medical Director (Medical Monitor)

Remote, Malaysia +3 locations 2 postings

Purpose: Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are …

Added Oct 16, 2026

Save job

Amgen

Global Insights Senior Manager - Oncology

Thousand Oaks, California, United States +1 location

Full time
Regular

… that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Global Insights Senior Manager - Oncology What you will do Let’s do this. Let’s change the world. In this vital role you will be …

Added Oct 16, 2026

Save job

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

Save job

IQVIA Holdings

CRA/Sr CRA -Sponsor dedicated-Bulgaria

Sofia, Bulgaria

… the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Managing progress by tracking …

Added Oct 15, 2026

Save job

Gilead Sciences

Associate Director, Market Access and Reimbursement - Kite

Uxbridge, United Kingdom

Full time
Regular

Associate Director, Market Access and Reimbursement, Kite Kite, a Gilead Sciences company, has successfully launched …

Added Oct 15, 2026

Save job

Amgen

Global Insights Senior Manager - Xaluritamig

Thousand Oaks, California, United States

Full time
Regular

Added Oct 15, 2026

Save job

Thermo Fisher Scientific

CRA I/CRA II/Sr CRA

Singapore, Singapore

Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top …

Added Oct 16, 2026

Save job

Zoetis

Senior Diagnostics Solutions Consultant

US FL Remote

Full time
Regular

… new business leads and referrals, including competitive placements and opportunities in academia/research settings. ● Collaborate cross-functionally (sales, accounting, technical support) to ensure customer …

Added Oct 20, 2026

Save job

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 …

Added Oct 16, 2026

Save job

Thermo Fisher Scientific

FSP Sr. CRA (Oncology & Cell Therapy)

Remote, Singapore

… 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 …

Added Oct 16, 2026

Save job

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

Save job

Thermo Fisher Scientific

CRA II / Sr CRA - FSP - Austria

Vienna, Vienna, Austria

View job

Save job

About this opportunity

Original employer description

Work Schedule

Other

Environmental Conditions

Office

Job Description

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 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 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.

What You’ll Do:
• 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.

Education and Experience Requirements:
• 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.

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

Why this result? · Employer labels

Keywords also found in description

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