Clinical Research Associate
$61.3k - $122.7kAbbott
Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity Our Core Lab business unit currently has an opportunity for a Clinical Research Associate. This role is based remote in the United States near a major airport or in an Abbott Office approved. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers. What You’ll Work On As a Clinical Research Associate (CRA), you will support clinical trial sites from study start-up through closeout, ensuring studies are conducted in compliance with protocols, regulatory requirements, and company procedures. This role reports to the Clinical Manager and partners with Clinical Project Teams and Operations leadership. The successful candidate will work in a regulated quality environment, manage assigned tasks and timelines, build cross-functional relationships, and contribute to study success under general supervision. Key Responsibilities Conduct site qualification, initiation, monitoring, and closeout visits. Provide training and support to investigators, study coordinators, and site staff. Monitor protocol compliance, data quality and Good Clinical Practice (GCP) requirements. Review source documents and verify clinical study data for accuracy and completion. Ensure only eligible participants are enrolled in studies. Manage and maintain study and regulatory documentation. Monitor investigational product accountability and inventory. Review adverse event reporting for accuracy and compliance. Assess site performance, including patient recruitment and retention efforts. Prepare monitoring reports and communicate findings, risks, and corrective actions.Build strong relationships with clinical research sites and internal stakeholders. Develop knowledge of applicable clinical research regulations and study types. Required Qualifications Bachelor's (life sciences or clinical research preferred) or equivalent combination of education and work experience. Minimum 1-year clinical research experience required. Must be detail-oriented and efficient in time management. Must have excellent written and verbal communication, organizational and presentation skills. Must be able to work effectively with others. Self-directed and able to work within a fast paced and constantly changing environment. Ability to multitask, prioritize, and manage time efficiently. Proficient computer skills, including Microsoft Office Suite (Word, Excel, Outlook, etc.). Travel: 40 % Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at abbott.com, on LinkedIn at and on Facebook at The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted. #J-18808-Ljbffr Abbott
- ...autoimmune disease, with unmet medical needs worldwide. InnoCare has built up a fully integrated platform in terms of research and development, clinical development, manufacturing and commercialization. To date, the Company has developed a robust product pipeline...SuggestedWorldwide
$74.5k - $197.5k
...visits) in accordance with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive, and track... ...of independent on-site monitoring experience as a Clinical Research Associate (CRA) in a CRO, sponsor, or similar setting. • Equivalent combination...SuggestedFull timePart timeLocal areaImmediate startWorldwide- ...Job Title 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 and assist...Suggested
$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...SuggestedTraineeshipLocal area$47.03k - $66.3k
...human condition through medical education, scientific research, and direct patient care. At NYU Langone Health, equity... ...exciting opportunity to join our team as a Research Associate. This role involves clinical research data collection, interaction with human subjects...SuggestedDaily paidFull timeCasual workRemote workDay shiftAfternoon shiftEarly shift- The Mount Sinai Health System in New York, NY seeks a Clinical Research Associate I to monitor all aspects of the clinical trial life cycle, from site management through study closure, across Phases I-IV and post-marketing studies. Responsibilities include preparing essential...
- Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team (remote; with travel). As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues...Work at officeRemote workFlexible hours2 days per week
- Be the connection between science and solutions. As a Clinical Research Associate, you will take the next step in your clinical research career, supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals...InternshipRemote workFlexible hours
- ...therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory... ...from direct line management. We are now recruiting Clinical Research Associate II to join our team in the Netherlands. This is a remote...Local areaRemote workNight shiftDay shift
- Clinical Research Associate - Oncology - OH/PA/VA At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development...WorldwideFlexible hours
- 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, evaluate...RelocationVisa sponsorship
- ...disorders are treated. Join us in building the next generation of personalized neuroscience-based therapeutics. Primary Role The Clinical Research Associate (CRA) is responsible for the oversight of assigned investigative sites in accordance with all applicable protocols,...Interim roleRemote work
- Position Summary The Clinical Research Associate (CRA) is responsible for monitoring clinical trial sites to ensure studies are conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and applicable...Work at officeLocal areaFlexible hoursAfternoon shift
- Job Title: Clinical Research Associate II (CRA II) Job Location: United States - Remote Job Overview: The Clinical Research Associate II (CRA II) is responsible for monitoring assigned investigational sites throughout the clinical trial lifecycle. The CRA II serves as the...Interim roleRemote work
- ...interest in fighting cancer. General Description: The CRA executes clinical monitoring activities at clinical trial sites and monitors... ...clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines At least 2 years of (CRA) monitoring...Local area
- POSITION TITLE: Clinical Research Associate II DEPARTMENT: Monitoring Ora Values the Daily Practice of … Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor At Ora, we are building the future of ophthalmic clinical research. As the world...Daily paidFull timeInterim roleLocal areaRemote workFlexible hours
$4,000 - $9,000 per month
...Clinical Research Associate DotLab is transforming the diagnosis and management of endometriosis, a disease that affects 1 in 10 women worldwide and currently requires surgery to diagnose. The disease is the cause of over half of unexplained infertility, and is a primary...Work experience placementWork at officeRemote workWorldwideFlexible hours- ...treatment technologies, specifically focusing on advanced and interventional oncology for breast cancer clinical studies is hiring a Remote Clinical Research Associate to work in the United States. As a Clinical Research Associate (CRA), you will play a key role in...Work at officeRemote work
$50.5k - $82.01k
...nurses, business people, tech experts, researchers, and systems analysts to advance our mission... ...within the MGB Cancer Institute Clinical Trials Office is seeking candidates experienced... ...Multicenter Senior Clinical Research Associate/Monitor (Sr. CRA) coordinates a...Work at officeLocal areaRemote workShift work- We are working with a fast growing organization who is seeking to bring on experienced Clinical Research Associates located nationwide. The role requires limited to no travel and offers a tremendous opportunity to partner with a growing, high-quality and innovative team...Interim role
- ...all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical... .... Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research...Work from homeHome office
- ...monitoring and site education. CRAs are to complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines,... ...clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines Excellent communication and...Local area
$62.6k - $97.1k
...patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists... ...to conduct innovative translational and clinical research that is driving a revolution in... ...team as a Clinical Research Associate ! This position offers the opportunity to...Full timeWork at office$97k - $193k
...Senior Clinical Research Associate position focusing on central nervous system and psychiatry studies. Manage research activities across multiple study sites in the Northeast and Mid-Atlantic regions, overseeing site selection, regulatory compliance, training, and study...Contract workWork at office- Syneos Health seeks an Experienced Clinical Research Associate (CRA) with at least 1 year of independent monitoring experience for a homebased role in the United States. The candidate will perform site qualification, initiation, monitoring, and close-out visits, ensuring...Remote job
- WOW Softech is seeking a Clinical Research Associate to join our global clinical trial program. Reporting to the Clinical Operations Manager, the candidate should have 5+ years of experience in clinical research and at least 3+ years of on-site monitoring or site visits...Remote job
- NYU Grossman School of Medicine is seeking a Research Associate to support clinical trials and cohort studies in dialysis centers across New York City. This per diem role requires flexible hours, including early mornings and evenings, and involves data collection, patient...Daily paidFlexible hoursAfternoon shiftEarly shift
- ...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...Contract workFor contractorsFreelanceImmediate startRemote work
- ...implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts,... ...a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside...Interim roleWork at officeWorldwide
- Fortrea seeks a Clinical Research Associate (CRA) to monitor sites across Europe and beyond, ensuring study conduct aligns with protocol and regulatory requirements. You will partner with investigators, initiate visits, monitor data quality, and support audits while advancing...Remote job
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