Clinical Research Associate
ICON Strategic Solutions
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 to shape the future of clinical development. What You Will Be Doing Serve as the primary point of contact between investigational sites and the sponsor Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out Ensure site compliance with ICH-GCP, SOPs, and regulations Maintain up-to-date documentation in CTMS and eTMF systems Support and track site staff training and maintain compliance records Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting Support subject recruitment and retention efforts at the site level Oversee drug accountability and ensure proper storage, return, or destruction Resolve data queries and drive timely, high-quality data entry Document site progress and elevate risks or issues to the clinical team Assist in tracking site budgets and ensuring timely site payments (as applicable) Collaborate with cross-functional partners including CTAs, LTMs, and CTMs You Are A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN Eligible to work in United States without visa sponsorship A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry Experienced monitoring hematology oncology clinical trials Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF A clear communicator, problem-solver, and collaborative team player Willing and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Georgia, Florida or North Carolina, near major HUB airports to support efficient regional travel 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. #J-18808-Ljbffr ICON Strategic Solutions
$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$71.9k - $189k
...out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. • i.e., Good Clinical Practice (GCP)...SuggestedFull timePart timeLocal areaImmediate startWorldwide- ...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
- 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...SuggestedRelocationVisa sponsorship
- 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...Suggested
- Clinical Research Associate I Required Qualifications Bachelor's degree (foreign equivalent or higher). In lieu of a Bachelor's degree, a combination of clinical/healthcare, medical type industry setting and/or human research experience totaling four (4) years full-time...Daily paidFull timeWork at officeLocal areaVisa sponsorshipWork visaShift work
$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$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$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- A leading clinical research organization in New York is seeking a Cancer Clinical Trials CRC I to support clinical trial operations under supervision. Responsibilities include data collection, patient recruitment, and managing informed consent processes. Applicants should...
- Summary In this Clinical Research Associate role (may be contract or full‑time employee), you will be responsible for monitoring the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported...Full timeContract workInterim roleLocal areaRemote work
$91.34k - $114.17k
Clinical Research Associate - Oncology - New York City 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 placementLocal areaVisa sponsorshipFlexible hours- ...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
$81.7k - $92.3k
...Title: Clinical Research Project Associate Location: Midtown Org Unit: Multisite IT Operations Work Days: Weekly Hours: 35.00 Exemption Status: Exempt Salary Range: $81,700.00 - $92,300.00 *As required under NYC Human...Local areaRemote work$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...Full timePart timeImmediate startWorldwide- ...requirements Prepare, organize and submit IRB documentation for clinical trials Process and submit IND safety reports as delegated by... ...clinical trial operations What you’ll bring 2-6 years of clinical research experience, including at least 2 years in regulatory affairs or...Local areaWork from homeFlexible hours
- 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...Flexible hours
- 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
$102k - $162k
Job TitleSenior Clinical Research AssociateJob DescriptionThe Senior Clinical Research Associate is responsible for developing comprehensive study plans/protocols, ensuring adherence to ISO/FDA regulatory requirements, Good Clinical Practice (GCP) guidelines, and study...Full timeWork at officeImmediate startRemote workWork visa3 days per week- ...management activities to ensure compliance with regulatory standards. The successful candidate will leverage their knowledge of Good Clinical Practice and manage site-related activities while supporting patient recruitment. Join a passionate team dedicated to making a...
- ...for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred. Job Purpose 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 areaRemote workFlexible hoursShift work
- ...Clinical Research Associate I 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...TraineeshipLocal area
$56k - $70k
A leading medical center in Bronx, New York, seeks a Research Associate to support the clinical trials team. Responsibilities include data collection, patient interaction, and assisting in the management of clinical research activities. Candidates should have a Bachelor...Full time- Orca Bio is seeking a Clinical Research Associate to monitor the progress of clinical studies, either on-site or remotely. The ideal candidate will have a BA/BS and at least 2 years of CRA experience, with a preference for those experienced in oncology or hematology. Key...Remote job
$105k - $117k
A leading clinical outsourcing company seeks an Experienced Ophthalmology & Gen Med CRA 2 to join their Full Service Outsourcing team. This role involves extensive site monitoring, collaboration with study teams, and ensuring patient protocol compliance. Candidates should...Remote work- A biotechnology company is looking for a Senior Clinical Research Associate to oversee clinical trials in the United States. The position requires extensive experience in clinical research, particularly in oncology, with responsibilities including site management, regulatory...Remote job
- Overview Experienced Clinical Research Associate - Full-Service 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...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- A leading healthcare organization is seeking a Clinical Research Associate in Connecticut to monitor oncology studies and ensure compliance at investigational sites. The ideal candidate will have a Bachelor's degree in Life Sciences or be a qualified RN, with 2+ years of...Remote work
- 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
- Medpace, Inc. is seeking a full-time Clinical Research Associate for their team in Georgia. This position offers the unique opportunity to be involved in every stage of the drug development process while working remotely. Ideal candidates will hold a relevant degree and...Remote jobFull time
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