Clinical Research Associate [Remote]
Icon Clinical Research
- Remote job
Clinical Research Associate - Central
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 analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. Our client is looking for candidates with experience monitoring Ophthalmology trials or multi-TA.
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
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
$71.9k - $189k
...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...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...SuggestedContract workInterim roleLocal areaImmediate startRemote workFlexible hours
$66.9k - $100.3k
...Description Clinical Research Associate I Reports To: Sr. Manager, CA Site Ops Position Summary The Clinical Research Associate I (CRA) works in parallel with Clinical Trial Managers to manage clinical studies conducted by bioMerieux. The CRA is the primary liaison between...SuggestedTemporary workLocal areaRemote workWork from homeFlexible hours- ...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...Suggested
- ...Job SummaryUnder general supervision, the clinical research associate (CRA) will be responsible for oversight of clinical trials for the SLU School of Medicine. Responsibilities include screening, recruiting and enrolling subjects, conducting subject research visits, providing...SuggestedWork at office
- ...Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All RegionsICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity...
- ...Direct message the job poster from Integrated Resources, Inc ( IRI ) Lead Recruiter at Integrated Resources Inc. (IRI) Sr Clinical Research Spec 100% remote in CA/MN 12 Months+ Preferred location(s): Santa Rosa, CA / Northern California - Bay Area / Plymouth,...Contract workRemote work
- ...A clinical research organization is seeking a Senior Regional Site Manager in the Kansas City area to oversee clinical trials at investigative sites. The Senior RSM will ensure data quality and integrity while managing relationships with clinical investigators and site...
$87.2k - $169.3k
...Senior CRA 1IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across... ...Coast, US.Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful...Full timePart timeImmediate startWorldwide$75.48k - $94.35k
Excellent written and verbal communication in English Clinical Research Associate- West 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...Work experience placementFlexible hours$71.9k - $189k
...or healthcare. Responsibilities include conducting site visits, administering training to sites, and ensuring compliance with clinical research regulations. The position offers a potential base pay between $71,900 and $189,000, based on qualifications and experience. #J...- Experienced Clinical Research Associate - Sponsor Dedicated Updated: Yesterday Location: Remote, MO, United States Job ID: 25109784-OTHLOC-1500-2DMO-2DR Description Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health® is a leading fully integrated...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions 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...Flexible hours
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region 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...Work experience placementLocal areaVisa sponsorshipFlexible hours- ...Company Description Medicine moves forward here. So will you. Clinical trials, safety studies, and audits make safe and innovative pharmaceutical... ...a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting. We are diverse in...Interim roleRemote work
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good...Local areaRemote work
- Syneos Health is seeking an Experienced Clinical Research Associate - Sponsor Dedicated. The role focuses on site qualification, initiation, interim monitoring, and site management to ensure regulatory and protocol compliance, with on-site or remote work in the US. You...Remote jobInterim role
- bioMérieux in Hazelwood, MO is seeking a Clinical Research Associate I to support clinical studies under supervision. The CRA serves as liaison with site personnel, helps ensure studies meet regulatory and protocol requirements, and contributes to study procedures and documentation...Remote job
- We are looking for a FREELANCE, PART-TIME CRA to strengthen our clinical operations team in Ventura, Illinois & Ohio! Job Requirements... ...of onsite monitoring activities Profound knowledge of clinical research processes and medical terminology Expert knowledge of ICH GCP,...Part timeFreelanceLocal areaRemote work
- Washington University in St. Louis is seeking a Clinical Research Study Assistant II in Emergency Medicine to support protocol-driven activities on campus. You will screen participants, obtain informed consent, enroll eligible subjects, and coordinate visits and documentation...
- bioMérieux is seeking a Clinical Research Associate I to partner with Clinical Trial Managers, coordinating site activities, monitoring studies, and ensuring regulatory compliance. The role serves as the primary liaison for study sites, handling specimen logistics and data...
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes. Job Responsibilities Perform site qualification, site initiation, interim monitoring...Interim roleLocal areaImmediate startRemote workFlexible hours
- AbbVie is seeking a field-based Clinical Research professional to oversee site engagement across multiple sites in the US. You will train investigators, monitor site performance, and ensure protocol compliance while maintaining data integrity and patient safety. Responsibilities...
$90k - $130k
..., GA, KS, MA, MD, MI, NC, OH, OK, TN, TX, WA Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA. Our... ...clinical data at assigned sites. The Clinical Research Associate (CRA) will execute monitoring responsibilities for clinical...Permanent employmentFull timeContract workInterim roleWork at officeRemote workFlexible hours- Syneos Health seeks a Clinical Research Associate - Full-Service to support global trials in a fully remote capacity. The role focuses on site qualification, monitoring visits, IP handling and ensuring GCP/ICH compliance across investigator sites. The CRA will collaborate...Remote job
- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to manage site operations, ensuring compliance with regulations. This role includes performing site qualification, monitoring, and documentation activities. The ideal candidate...Remote job
- bioMérieux in Missouri seeks a Clinical Research Associate I to support site coordination of clinical studies under supervision. You will liaison between sites and study team, ensuring protocol compliance and timely data management. This role involves on-site and remote...Remote work
- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to manage site activities focusing on regulatory and protocol compliance. The role requires a Bachelor's degree in a related field and strong communication skills, with responsibilities...Remote job
$87.2k - $169.3k
...Senior CRA 1 IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across... ..., US. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful...Full timePart timeImmediate startWorldwide- A leading healthcare organization in Kansas City is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities ensuring compliance with protocols and quality standards. The ideal candidate will possess an advanced degree, extensive CRA experience...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Associate [Remote]. Be the first to apply!
- on-site clinical research associate (traveling/remote) Missouri
- senior devops engineer remote Missouri
- remote medical coding supervisor Missouri
- remote virtual Missouri
- remote contract attorney Missouri
- clinical data manager remote Missouri
- remote servicenow developer Missouri
- online remote Missouri
- remote junior web developer Missouri
- remote work no experience Missouri

