Clinical Research Associate, Single Sponsor dedicated in Poland
IQVIA Holdings
Clinical Research Associate IQVIA is hiring Clinical Research Associates! Join IQVIA today and make an impact on patients' outcome! Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Responsibilities Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Qualifications Minimum of a Bachelors Degree in scientific discipline or health care. Experience of 1 year in on-site monitoring clinical trials. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of Polish and English language. Ability to establish and maintain effective working relationships with co-workers, managers, and clients. Connect to great opportunity™ IQVIA™ is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 119.400,00 zł - 280.000,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA Holdings
$71.9k - $189k
...applicable regulations and guidelines, and sponsor requirements. Essential Functions •... ...with contracted scope of work and Good Clinical Practice. • Work with sites to adapt,... ...skill in applying, applicable clinical research regulatory requirements. • i.e., Good...SuggestedFull timePart timeLocal areaImmediate startWorldwide- Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to...SuggestedContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Overview Clinical Research Associate (II - Sr) - Sponsor Dedicated - Home-Based & Regionally Aligned Across US & CAN Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical,...SuggestedWork at officeRemote workWork from homeFlexible hours
$125k - $145k
...Health? Join our global team dedicated to innovation and initiative,... ...regulatory requirements, i.e. Good Clinical Practice (GCP) and... ...medidata as necessary. Supports research sites with local Institutional... ...and acts as referent for the sponsor. Consistently prepares accurate...SuggestedContract workLocal areaRemote workFlexible hours$110.52k - $138.15k
...Senior Clinical Research Associate – Oncology – New York ICON plc is a world‑leading healthcare intelligence... ...Experience supporting sites and/or sponsors in regulatory inspections Experience... ...to our culture and values. We’re dedicated to providing an inclusive and accessible...SuggestedWork experience placementInterim roleLocal areaRemote workFlexible hours- ...Clinical Research Associate - Oncology - GA, FL or NC ICON plc is a world-leading healthcare intelligence... ...investigational sites and the sponsor Conduct all types of site visits, including... ...to our culture and values. We’re dedicated to providing an inclusive and accessible...Local areaVisa sponsorshipFlexible 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$71.9k - $169.3k
...Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile,... ...patients faster. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring...Full timePart timeImmediate startWorldwide- ...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
- ...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...
$24 - $26.92 per hour
...Description Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading... ...Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration... ...growth and learning A team dedicated to improving lives through innovation...Hourly payWork at officeFlexible hours$38 - $40 per hour
...the job poster from Baim Institute for Clinical Research Director, Human Resources at Baim Institute... ...Research The Sr. Clinical Research Associate/Field Monitor Contractor performs remote... ...for audits (Regulatory Agency, Sponsor, etc.). Attend Baim CRA meetings. Demonstrate...Part timeFor contractorsInterim roleRemote workWork from home10 hours per week$91.34k - $114.17k
...world-leading healthcare intelligence and clinical research organization. We’re proud to foster an... ...currently seeking a Clinical Research Associate to join our diverse and dynamic team.... ...to our culture and values. We’re dedicated to providing an inclusive and accessible...Work experience placementFlexible hours- ...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
$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- ...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
- ...Summary Shape the Future of Research Administration at the... ...Us? The Office of Sponsored Projects... ...Research Administrator Associate . This vital role supports... ...negotiation collaboration with clinical trial study teams to... ...Administration as the next dedicated Research Administrator...Contract workWork at officeImmediate startRemote workMonday to FridayFlexible hoursShift work
- ...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...
- ...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
$11.5 per unit
...5 years old with prior pet care experience, strong communication skills, and reliable transportation. Compensation starts at $11.50 per appointment plus $2 for fuel, totaling approximately $17.25 per hour. Join a supportive team dedicated to pet care. #J-18808-Ljbffr...Hourly payFlexible 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
$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
$91.5k - $137.3k
...implementation, on-site monitoring of clinical research studies as well as on-going site management... ...protocol. Verifies issues or risks associated with blinded or randomized information... ...attends Investigator Meetings and/or sponsor face-to-face meetings. Participates in...Contract workLocal areaRemote workNight shift$30 - $50 per hour
About the job Data Entry Clerk - No experience Only US citizens will apply. Applications from other countries are not acceptable. Data Entry Clerk - No experience We are an online retailer located in a small office/warehouse in New York, NY, We...Hourly payWork at officeMonday to FridayFlexible hoursShift 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- ...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
- ...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
- ...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...
- ...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...
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