Clinical Research Associate II
ICON
Clinical Research Associate II (FSP - Sponsor Dedicated) 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 and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. 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: 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 on site. Mandatory advanced English 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 35%) Based in Buenos Aires. -- Note: This is a Remote position based in Buenos Aires, Argentina only -- #LI-Remote 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 ICON
- Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health® is a leading fully integrated biopharmaceutical solutions organization... ...assigned training as required. For Real World Late Phase, the CRA II will use the business card title of Site Management...SuggestedInterim roleLocal areaImmediate startRemote work
- ...influence and impact when it matters most and support from direct line management. We are hiring a Senior Clinical Research Associate/ Clinical Research Associate II, this position will be fully home based working in the UK or Northern Ireland. About you: You are calm,...SuggestedRemote workWork from homeNight shift
- Syneos Health is seeking a CRA II in Germany to perform site qualification, initiation, on-site or remote monitoring, and close-out visits, ensuring adherence to ICH-GCP and regulatory standards. You will coordinate with trial sites across the DACH region and manage data...SuggestedRemote job
$125k - $140k
...What You Will Do You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in... ...trials and respond to emergency situations based upon clinical research standards. Responsibilities Responsible for all aspects of study...SuggestedWork at officeLocal areaNight shift- ...Piper Companies is seeking a Clinical Research Associate to support a leading organization within the pharmaceutical/biotechnology industry located... ...date. Keywords: Clinical Research Associate, CRA, CRA II, Senior CRA, Clinical Monitoring, Independent Monitoring, Site...SuggestedInterim roleRemote workNight shift
$75k - $95k
...players in biopharma and translational research. We’re bringing the best minds together... ...it happen, from hospital labs to mobile clinics. By helping providers, patients, and families... ...Role Overview The Clinical Research Associate II is responsible for set-up, initiation,...Hourly payContract workWork experience placementRemote workWork from homeWorldwideNight shift$40k - $55k
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- Supporting innovative translational neuroscience research, the full-time Research Assistant II will engage in wet laboratory, animal research, and clinical trial operations, collaborating with multidisciplinary teams to advance cancer care. Key responsibilities Ensure...Full timeWork experience placement
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Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support oncology clinical trials for a well-established organization within... ...This individual will play a critical role overseeing Phase II and Phase III oncology studies, often functioning as the...Contract workRemote work$91.34k - $114.17k
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...Worldwide- Comagine Health is seeking a thoughtful Research Associate II to join the Research and Evaluation Team. The role involves managing and implementing research studies and evaluation projects, with emphasis on applied research and program evaluation to inform public health...Remote job
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...both technology development and biological research projects. The role will involve... ...Responsibilities Perform molecular biology workflows associated with DNA and RNA sequencing, including... ...in an academic, biotechnology, or clinical molecular biology laboratory; Experience...For contractors$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...Full timePart timeLocal areaImmediate startWorldwide$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...Daily paidFull timeCasual workRemote workDay shiftAfternoon shiftEarly shift$24 - $29 per hour
...Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the... ...the site level. Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative...Hourly payWork at officeFlexible hours$100k - $125k
...Piper Companies is seeking a Clinical Research Associate to support a growing client in the pharmaceutical industry in the United States. The Clinical Research Associate role is fully remote with regional travel required to clinical trial sites. The Clinical Research Associate...Remote work- IQVIA is seeking a Site Monitor to oversee study sites in New Jersey, ensuring data are reported per protocol and regulatory standards. You will conduct visits and coordinate with sites under GCP guidance. Role requires at least 2 years of on-site monitoring, strong English...
$155k - $175k
...Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry. The Clinical Research Associate (CRA) role is ideal for an experienced monitor...Interim roleRemote work- ...Senior Clinical Research Associate (CRA) overseeing clinical trial operations for cell therapy programs, including tumor infiltrating lymphocyte (TIL) therapies, with a focus on solid tumors. Responsibilities manage study start-up conduct on-site monitoring visits oversee...Remote work
$110k - $175k
...Stifel Stifel strives for a culture that puts its clients and associates first: a culture where everyone belongs, everyone is welcome,... ..., modeling, and organizational support to the senior level Research Analysts. Has mastered the foundational skills required of an...Local areaFlexible hours$150k - $200k
...Stifel Stifel strives for a culture that puts its clients and associates first: a culture where everyone belongs, everyone is welcome,... ..., modeling, and organizational support to the senior level Research Analysts. Has mastered the foundational skills required of an...Local areaFlexible hours- ...final disposition. Responsibilities include compiling, analyzing, redacting, and reproducing documents for discovery, filing, legal research, witness communication, and assisting ADAs in court and at trials. A NY driver’s license with at least two years of driving...Work at office
$47.23 - $75.59 per hour
...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... ...an experienced Laboratory Technologist II to join our Main Hospital Rapid Results...Monday to FridayFlexible hoursShift workNight shift- ...Abbott is seeking a Clinical Research Associate I for a remote role in the United States. You will support clinical trial sites from start-up through closeout, ensuring compliance with protocols and regulatory requirements. Role reports to Clinical Manager and involves...Remote work
- ...Role: Clinical Research Associate (CRA) responsible for site performance and compliance in a specified country, managing all phases of clinical trial conduct at assigned sites. Objectives: ensure adherence to ICH-GCP, local regulations, and company policies, while fostering...Work experience placementLocal areaRemote work2 days per week3 days per week
$22 per hour
...have a positive impact JOB SUMMARY: As a Lab Technician II within our Lab Operations division, you will play a vital role in... ...’s core values including respect, diversity, sustainability, research, and service. Adhere to iAnthus' cultural principles of collaboration...Full timeTemporary workLocal areaFlexible hoursShift 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...
- 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
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