Clinical Research Associate (f/m/d) EMEA
ZOLL Medical
Clinical Research Associate (CRA) (f/m/d) Remote (EMEA) The Cardiac Management Solutions division of ZOLL Medical Corporation develops products to protect and manage cardiac patients, including the LifeVest® wearable cardioverter defibrillator (WCD), the ZOLL cardiac monitor, and associated technologies. The LifeVest is a wearable defibrillator worn by patients at risk for sudden cardiac arrest (SCA), providing protection during their changing condition and while permanent SCA risk has not been established. The LifeVest allows a patient's physician time to assess their long-term arrhythmic risk and make appropriate plans. Our mission: "Saving more lives!" Our EMEA team is looking for a dedicated and motivated Clinical Research Associate (CRA) to support us in the execution and monitoring of clinical trials. In this role, you will play a key part in ensuring the quality and integrity of our clinical research projects from planning through to implementation. Areas of Responsibility: Monitoring and site management activities for clinical research projects Acting as liaison between the company and clinical sites to resolve any site-related issues quickly and effectively Preparation of study-related documents including but not limited to informed consent forms, Notes to File, etc. Monitor ongoing compliance with study protocols and site adherence to global regulatory guidelines, including safety reporting Responsible for the distribution, collection and tracking of regulatory documentation and support regulatory submissions Support clinical operations management in project management Partner with cross-functional teams (EMEA and US) such as data management and medical affairs with query management, data reviews and resolution Coordinate or manage multiple projects across multiple centers and countries Travel to study sites based on project needs Perform other duties as assigned by management Ability to travel up to 65%, based on project needs, including national and international conferences and responsibilities Participate in research meetings including presentations at those meetings Experience and Personal Qualities: MS/PhD in a clinical, scientific, or related field; and ideally 3+ years of experience in the medical industry Cardiology experience preferred Strong working knowledge of medical/scientific terminology and working knowledge of Ministry of Health regulations and GCP guidelines is required Knowledge of the legal and regulatory landscape concerning clinical research Professional proficiency in English (written and spoken) and one other major European language (preferably French, Italian or Spanish) Demonstrated proficiency in implementing, monitoring, and management of clinical trials (start-up to close-out) Presentation skills Proficient in Microsoft Office, including Word, Excel, and Project What We Offer: A meaningful mission – helping to save lives every day An innovative work environment where you can take ownership and make a real impact on our success A diverse role with strong growth and development opportunities in a dynamic and expanding medical technology market Flexible working hours and 30 days of annual leave to support your work-life balance A comprehensive benefits package, including a company pension scheme, supplementary health insurance, sports and wellness programs, an Employee Assistance Program, corporate benefits, and unique employee events Training and development opportunities to support your professional and personal growth Saving more lives together! If you would like to become part of our mission, we look forward to receiving your application via our careers page. To apply, all we need is your CV. A cover letter or additional documents are not required, but you are welcome to submit them if you wish. Your contact person Transparency and open communication are important to us. If you have any questions about the position or the application process, please do not hesitate to get in touch. Your contact for this role is: Tim Schneider HR Business Partner Phone: View phone number on click.appcast.io Email: View email address on click.appcast.io ZOLL Medical
- ...out visits) in accordance with contracted scope of work and Good Clinical Practice. Work with sites to adapt, drive, and track subject... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and...SuggestedLocal area
$91.34k - $114.17k
...ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...Advert Posting We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research...SuggestedWork experience placementFlexible hours- ...Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate...Suggested
$71.9k - $169.3k
...trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you...SuggestedFull timePart timeImmediate startWorldwide$110.52k - $138.15k
...Sr. Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of...SuggestedFlexible hours$103k - $130k
...Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate (Sr. CRA) is responsible for the set‑up, initiation, execution, monitoring and close‑out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The...Contract workRemote workNight shift$38 - $40 per hour
...exclusive features. Direct message the job poster from Baim Institute for Clinical Research Director, Human Resources at Baim Institute for Clinical Research The Sr. Clinical Research Associate/Field Monitor Contractor performs remote and on-site visits, such as, Qualification...Part timeFor contractorsInterim roleRemote workWork from home10 hours per week$108.7k - $139.8k
...All Jobs Senior Clinical Research Associate The Senior Clinical Research Associate is a senior individual contributor and leader within the EBR Clinical organization, accountable for monitoring excellence, data integrity, and site engagement across the full lifecycle...Contract workWork at officeRemote workNight shift$110.52k - $138.15k
...Senior Clinical Research Associate – Oncology – New York ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission...Work experience placementInterim roleLocal areaRemote workFlexible hours$125k - $145k
...work, Alira Health SOPs and regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH... ...utilizing the filing index and medidata as necessary. Supports research sites with local Institutional Review Board (IRB)/Ethics...Contract workLocal areaRemote workFlexible hours- ...A medical device company focused on cervical spine conditions is seeking a Clinical Research Associate. Responsibilities include managing clinical trials, ensuring compliance, and coordinating operations with study sites. The ideal candidate will have 3-5 years of clinical...Remote work
- ...EPM Scientific is currently partnering with a leading Cardiovascular Medical Device company that is seeking an experienced Clinical Research Associate Contractor on a remote basis. Key Requirements Proven experience as a CRA within the cardiovascular medical device field....Contract workFor contractorsFreelanceImmediate startRemote work
- ...Summary The Breast Center at Baylor College of Medicine is seeking a skilled Clinical Research Associate. The ideal candidate will facilitate communication between requestors and providers of breast cancer-related human biospecimens. The Coordinator executes the decisions...
- ...Bright-Uro, based in the U.S., is seeking a Clinical Research Associate I to provide support for clinical studies. This role involves significant travel, requiring on-site visits throughout the Midwest, contributing to the quality and integrity of various research projects...
$115k - $125k
...Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote permanent position located based out of CST . The Clinical Research Associate (CRA) will travel to sites 8-10 days out of the...Permanent employmentWork at officeRemote work- ...Bright Uro is seeking a Clinical Research Associate I (CRA I) to join their dynamic team. This entry-level role offers exposure to the full lifecycle of clinical studies, including oversight at investigational sites and data collection. Candidates must be detail-oriented...Work at office
- ...Objective As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial role in the execution and management of Phase 1, Phase 2, and Phase 3 clinical trials. You will collaborate closely with cross‑functional teams to ensure adherence...Interim roleLive inLocal areaRemote work
$58.66k - $81.68k
...Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre‑clinical, Phase I through Phase IV, and post‑marketing studies....Traineeship- ...A healthcare organization is seeking a Research Associate to work with Principal Investigators in clinical research studies. Responsibilities include overseeing data integrity, managing study information, and preparation of research presentations. Candidates should have...
- ...Overview As a clinical research associate (CRA), you are responsible for completing clinical research and administrative tasks for clients. You facilitate documentation for clinical research. As a CRA, you monitor clinical tasks for correct functioning and completion,...RelocationVisa sponsorship
$91.5k - $137.3k
...involving start-up and study implementation, on-site monitoring of clinical research studies as well as on-going site management. Incumbents work... ...according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies...Contract workLocal areaRemote workNight shift- ...Title: Clinical Research Associate This role is located in either New York or New Jersey The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works...Hourly payTemporary workLocal areaRemote work
- ...language model-based system built to understand and assess clinical characteristics in EMRs. Synapsis AI is designed for installation... .... As a vital member of our diverse team, our Clinical Research Associates (CRA) will collaborate closely with the AI Research and software...Local areaFlexible hoursShift work
- ...A leading healthcare organization in New York is seeking a Research Associate to oversee clinical trials. The role requires strong clinical research skills, a Bachelor's degree, and GCP training. Responsibilities include managing daily trial activities, ensuring compliance...
- ...A leading healthcare organization in New York is seeking a Clinical Research Associate (CRA) to oversee clinical trials and ensure compliance with regulations. This role requires a degree in a scientific discipline and experience in the healthcare sector. Key responsibilities...Visa sponsorship
- ...Clinical Research Associate - Oncology - GA, FL or NC ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission...Local areaVisa sponsorshipFlexible hours
- ...The Position The Position (Phase 1 healthy volunteer studies): CRA/Sr. CRA drives quality clinical research and delivery of monitoring and site management activities, ensuring patient safety/rights and wellbeing, data reliability, scientific integrity, and regulatory/process...Local areaRemote workNight shiftWeekend work
$103k - $130k
...players in biopharma and translational research. We're bringing the best minds together... ...it happen, from hospital labs to mobile clinics. By helping providers, patients, and families... ...possible. The Sr. Clinical Research Associate (Sr. CRA) is responsible for?set-up,...Hourly payContract workRemote workWork from homeWorldwideFlexible hoursNight shift- A leading hospitality tech firm is seeking an experienced Product Marketing Manager to drive their Go-to-Market strategy and marketing execution. This role involves deep regional market expertise, developing compelling product messaging, and close collaboration with sales...Emea
$34 - $36 per hour
...Immigration Coordinator to manage international work visa cases for an AI research client. The role requires 6+ years of immigration coordination... ..., with strong knowledge of work visa processes across APAC and EMEA. This position is crucial for compliance and requires strong...EmeaHourly payWork visa
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