714 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.
TFS
Thermo Fisher Scientific +1 location
… 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 …
Added Oct 16, 2026
+1 location
Pay posted by employer $156,900–$247,000
At our company, we aspire to be the premier research -intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health …
Added Oct 16, 2026
We're hiring a Senior Manager / Associate Director into our Solids Development (SOliD) department within Drug Product Research & …
Added Oct 15, 2026
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Thermo Fisher Scientific +2 locations 6 postings
… Ability to travel internationally as required. Valid driving license. Short role description The Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and …
Added Oct 16, 2026
Pay posted by employer $155,540–$188,480
The Associate Director, Global Medical Neuroscience Medical Communications is a key contributor within the Global Medical …
Added Oct 15, 2026
TFS
Thermo Fisher Scientific
Join Us as a Senior /Principal Safety Specialist – Make an Impact at the Forefront of Innovation We have successfully supported …
Added Oct 16, 2026
TFS
Thermo Fisher Scientific
… 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
Delivers day-to-day customer service for clinical trial logistics requests, updates, and inquiries in accordance with established procedures, service levels, …
Added Oct 27, 2026
Pay posted by employer $155,540–$188,480
The Associate Director, Global Medical Neuroscience Medical Communications is a key contributor within the Global Medical …
Added Oct 15, 2026
+1 location
Pay posted by employer $142,400–$224,100
This position participates in the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your advanced leadership and …
Added Oct 16, 2026
Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Senior Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure …
Added Oct 15, 2026
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Thermo Fisher Scientific
Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully …
Added Oct 16, 2026
+2 locations
… 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
+9 locations
As an Associate Principal at IQVIA, you will be responsible for managing or leading multiple engagements and ensuring …
Added Oct 15, 2026
+2 locations
… Let’s do this. Let’s change the world. In this vital role you will report to the China Quality Compliance, Associate Director, JAPAC Quality within Clinical & Research Quality (CRQ). The Quality Compliance Lead provides …
Added Oct 15, 2026
TFS
Thermo Fisher Scientific
… 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
TFS
Thermo Fisher Scientific +5 locations
… 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
TFS
Thermo Fisher Scientific
… 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
+2 locations
… 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
Senior Manager, Value Strategy & Marketing - UPLIZNA & Oncology The Senior Manager, Value Strategy & Marketing …
Added Oct 15, 2026
TFS
Thermo Fisher Scientific +1 more
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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