Clinical Research Associate 2
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Clinical Research Associate- East Coast 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 clinical development. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60%) What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. #J-18808-Ljbffr
$71.9k - $189k
...accordance with contracted scope of work and Good Clinical Practice.• Work with sites to adapt,... ...care preferred. • Requires at least 2 years of year of on-site monitoring experience... ...skill in applying, applicable clinical research regulatory requirements.• i.e., Good...SuggestedFull timePart timeLocal areaImmediate startWorldwide$62.6k - $97.1k
...of all ages. Informed by basic research done at our Sloan Kettering... ...innovative translational and clinical research that is driving a revolution... ...team as a Clinical Research Associate ! This position offers the... ...organizational skills.Key Qualifications:1-2 years of clinical research...SuggestedWork at office2 days per week3 days per week$4,000 - $9,000 per month
...Clinical Research AssociateDotLab is transforming the diagnosis and management of endometriosis,... ...pain.DotLab is seeking a Clinical Research Associate to join our team and support DotLab... ...life sciences or related field required.2+ years of study monitoring (CRA) experience...SuggestedWork at officeRemote workWorldwideFlexible hours$120k
...Job Title Responsible for providing Clinical Research support for all clinical trials. Location: New York, New York, United States, 100... ...RN, BSN or equivalent Basic knowledge and adherence to GCPs 1-2 years of clinical research experience or equivalent experience...SuggestedFull timeWork experience placement- ...Fortrea is seeking a CRA 2 in the United States (Ohio, Pennsylvania, or Virginia) with at least 2 years of monitoring experience. Expect 8–10 on-site days per month, with a mix of onsite and remote work. The role focuses on site monitoring, data integrity, SAE handling...SuggestedLocal areaRemote work
- ...ICON plc is seeking a Clinical Research Associate II for the East Coast. You will design and monitor clinical trials, ensure protocol compliance and... ...% is expected. A Bachelor's in a science field and at least 2 years as CRA are required; knowledge of ICH-GCP; strong organizational...
$71.9k - $169.3k
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates... ...to patients faster.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the...Full timePart timeImmediate startWorldwide$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... ...for the Clinical Research Associate include: At least 2 years of onsite oncology monitoring experience Proficiency...Permanent employmentWork at officeRemote work$82.7k - $137.9k
...The Senior Clinical Research Associate I is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator... ...experience in clinical research site monitoring (preferably 2 years in Oncology) Preferred therapeutic experience in...Permanent employmentFull timeH1bLocal areaRemote workVisa sponsorshipWork visaRelocation packageWeekend work$58.66k - $81.68k
...Description Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities... ...Qualifications Bachelors Degree in life sciences or BSN. 1-2 years experience in relevant Clinical Research. Experience...TraineeshipLocal area$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Central/East (NY/NJ or TX) ICON is a global healthcare intelligence and clinical research organisation... ...nurse) or equivalent work experience required. ~2-5 years clinical monitoring experience required (CRA 2 for...Work experience placementLocal areaRemote workWork visa- Overview As a clinical research associate (CRA), you are responsible for completing clinical research and administrative tasks for clients. You facilitate... ...University degree in scientific discipline or health care 2-3 years experience in healthcare industry, and/or clinical...RelocationVisa sponsorship
$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... ...monitoring. Travel: May be expected to conduct 2-4 visits per month, travel regionally...Part timeFor contractorsInterim roleRemote workWork from home10 hours per week$103k - $130k
Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate (Sr. CRA) is responsible for the set‑up, initiation, execution, monitoring... ...research experience OR Doctoral degree in the field with 0-2 years clinical research experience. Basic knowledge of...Contract workRemote workNight shift$125k - $140k
...Oncology Sr. CRA 2 Our FSP team is currently seeking an Oncology Sr. CRA 2 with... ...will utilize your skills, knowledge, and clinical judgement to provide a high standard of care... ...emergency situations based upon clinical research standards. Responsibilities:...Work at officeLocal areaNight shift- ...Experience ~ High School Diploma/GED and 2 years work experience in Health Care. Preferred Education/Experience ~ Associate's Degree Health Care and 2 years work... ...AMT) is preferred American Society for Clinical Pathologist Certification (ASCP) is preferred...Work experience placementWork at officeNight shift
- ICON plc in Georgia seeks a Clinical Research Associate to monitor investigational sites and ensure ICH-GCP compliance. You will manage site visits,... ...southeast region. The role requires a Life Sciences degree (or RN), 2+ years of on-site monitoring experience, and ability to...
$96.2k - $151.4k
...phases of the trial. Performs clinical study site management/... ...Protocol, Site Monitoring Plan and associated documents. Gains an in-depth... ...them to develop strong clinical research capabilities. Travel Requirements... ...time. Expected travelling ~2-3 days per week. Current...Remote jobFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work2 days per week3 days per week- Clinical Research Associate - Cross Therapeutic Area - Georgia ICON plc is a world-leading healthcare intelligence and clinical research organization... ...visa sponsorship A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical...Local areaVisa sponsorshipFlexible hours
- ...Montefiore New Rochelle seeks a Research Associate I to oversee multiple clinical trials, acting as a primary contact for patients and study teams. The role involves coordinating with multiple departments to ensure timely completion of trial activities and adherence to...
- ...Montefiore Hudson Valley Collaborative seeks a Research Associate I to manage multiple clinical trials as a patient-facing liaison and trial team lead. You will work with departments hospital-wide to ensure timely completion of trial-related activities, maintaining protocol...
- ...Pulse Biosciences is seeking a Senior Clinical Research Associate to manage and monitor soft tissue ablation trials in the U.S. remote setup. The Sr. CRA will support study planning, site startup, patient recruitment, data quality, and regulatory compliance with CFR FDA...Remote work
- Job DescriptionCANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS: Illinois, Colorado, South Florida, New York, California, Houston, DallasThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the...
$60k - $80k
...searching for talented and passionate people who want to help shape the future of veterinary care. About the position The Vet Clinic Implementation Associate at Vetcove is responsible for overseeing the end‑to‑end management of large‑scale projects that enhance the customer...Hourly payFull timeRemote workHome office- ...ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Clinical Research Associate II to design and analyze clinical trials and interpret complex medical data to advance innovative therapies. You will conduct site qualification...
- ...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...
- ...Montefiore Orthopedics is seeking a Research Associate I to oversee multiple clinical trials. You will serve as the main point of contact for patients, families, and study teams, coordinating across hospital departments to ensure timely completion of trial activities....
- ...Syneos Health, Inc. is seeking a CRA II/Sr CRA for Germany (remote across Leipzig/Halle/Berlin) to monitor clinical sites. The role requires fluency in German and English, good regulatory knowledge, and the ability to manage remote and on-site visits. You will perform...Remote work
- ...organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to... .../patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies...Contract workInterim roleLocal areaImmediate startRemote workWork from homeFlexible hours
- ...Syneos Health, Inc. is seeking a Clinical Monitoring/CRA to support site management, monitoring, and data integrity across sponsor studies in a remote setup. The role emphasizes regulatory compliance and collaboration with cross-functional teams. The position requires...Remote work
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