Clinical Research Associate II Global Trials
$91.34k - $114.17kICON Strategic Solutions
CRA II - Adverum East 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. We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What You Will Be Doing 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 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. Experience in ophthalmology or gene therapy studies. Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license. 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. Salary range: $91,336.00-$114,170.00. 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
$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry for a remote... ...with investigative sites to ensure high-quality trial execution. Responsibilities Perform routine and close-...SuggestedPermanent employmentRemote work$91.5k - $137.3k
...Overview The CRA II is a seasoned, experienced... ...on-site monitoring of clinical research studies as well as on-... ...maintains study specific trial management tools/... ...Verifies issues or risks associated with blinded or randomized... .... Participates in global clinical monitoring/project...SuggestedContract workLocal areaRemote workNight shift$91.34k - $114.17k
CRA II - Adverum East ICON plc is a world-leading... ...intelligence and clinical research organization. We’re proud... ...a Clinical Research Associate to join our diverse... ...and analyzing clinical trials, interpreting complex... ...the years ahead. Global Employee Assistance Programme...SuggestedWork experience placementFlexible hours- ...A prominent clinical research organization in Philadelphia is seeking a Clinical Research support staff member to assist with clinical trials. The ideal candidate should have a BA, BS, RN, BSN, or equivalent, along with 1-2 years of clinical research experience. Responsibilities...Suggested
- ...ProTrials Research, Inc. is seeking a Contract Senior Clinical Research Associate to oversee clinical trial monitoring and management. This role involves ensuring compliance with protocols and SOPs while managing site personnel training and documentation. The ideal candidate...SuggestedContract work
- ...Clinical Research Associate I/II Benefits include: Medical, Dental, and Vision Insurance, 401(k), Stock Options NOTE: You must have a minimum of 3... ...managing operational aspects of the company’s ongoing clinical trials, in line with PMT’s corporate directives and under the...Local areaRemote workWorldwide
$84.5k - $162k
...pipeline by striving for excellence in clinical research, turning science into medicine for our... ...positioning AbbVie as the choice in clinical trials. Focus on site clinical research that... ...their development. May participate in global/local task forces and initiatives....Contract workTemporary workLocal area$56k
...Attorney’s Office has an opening for a Trial Preparation Assistant to support our Assistant... ...by NYC Police Dept. Perform legal research Engage in witness contact and... ...flexible spending account. COMMUNITY ASSOCIATE - 56057 Qualifications Qualification...Work experience placementWork at officeFlexible hours- ...Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic... ...level Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations...Work visa
- ...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...
- ...resources through Staff Augmentation, Global Talent Management, Value Added Services... ...professional excellence. Job Description Associate degree or higher preferred Experience:... ...industry or CRO Experience supporting clinical trials preferred Qualifications Knowledge, Skills...Permanent employment
- ...Syneos Health is seeking a CRA II based in São Paulo. This role involves performing site qualification, initiation, and management... ...The successful candidate will leverage their knowledge of Good Clinical Practice and manage site-related activities while supporting patient...
- 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...
- 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...
- ...Parexel International is seeking a Clinical Research Associate (CRA) to manage and monitor investigator sites for clinical trials in the United States. This role involves ensuring patient safety, compliance with regulations, and effective site management. The ideal candidate...
- ...Biopharmaceutical Research Company is seeking a detail-oriented Research Associate for a remote position focused on clinical and nonclinical research. The ideal candidate will have a Master... ...experience in supporting clinical trials. Responsibilities include study planning...Remote work
- ...Overview Experienced Clinical Research Associate - Full-Service Syneos Health is a... ...Self culture is what unites us globally, and we are dedicated to... ...contents of the ISF with the Trial Master File (TMF). Ensures the... ...Real World Late Phase, the CRA II will use the business card...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...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 work
- ...A medical device company focused on cervical spine conditions is seeking a Clinical Research Associate. Responsibilities include managing clinical trials, ensuring compliance, and coordinating operations with study sites. The ideal candidate will have 3-5 years of clinical...Remote work
- ...A well-established research institution in Pennsylvania is seeking a Clinical Research Assistant II for the GI Motility Frontier Program. The role involves providing technical and clinical support for various studies, including organizational tasks and data management...
- 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 looking for a Clinical Research Associate II (CRA II) in the United States. This role involves performing site qualification, site initiation, monitoring activities, and ensuring regulatory compliance. The ideal candidate will have a Bachelor's degree...
- ...A leading clinical research organization in New York is looking for a Clinical Research Associate to provide support for clinical trials. The role involves assisting with protocol design, site evaluations, and ongoing study monitoring. Candidates should have a BA, BS,...
$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$56k - $70k
Montefiore Health System is hiring a Clinical Research Coordinator I in Bronx, NY. This role involves supporting clinical trials, collecting and managing data, and ensuring compliance with study protocols. The ideal candidate will hold a Bachelor’s degree, with a preference...- ...ICON Strategic Solutions is looking for a Clinical Research Associate who will lead clinical trial monitoring with a focus on quality and continuous improvement. The individual will ensure adherence to protocols and conduct site visits to support successful trial execution...
$71.9k - $189k
...contracted scope of work and Good Clinical Practice. • Work with sites... ...available for filing in the Trial Master File (TMF) and verify... ..., applicable clinical research regulatory requirements. •... ...clients. IQVIA is a leading global provider of clinical research...Full timePart timeLocal areaImmediate startWorldwide- ...Clinical Research Associate I Required Qualifications Bachelor's degree (foreign equivalent or higher).... ...Qualifications Experience coordinating clinical trials in Oncology. Previous use of e-... ...OEA ( In accordance with the Title II Crime Awareness and Security Act, a copy...Daily paidFull timeWork at officeLocal areaVisa sponsorshipWork visaShift work
$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... ...month and be responsible for monitoring and clinical trials across the region for a leading Clinical Research...Permanent employmentWork at officeRemote work$75k - $85k
...About the Role You will be the operational backbone of our clinical trials. You’ll own the systems, documents, and workflows that... ...primary point of contact between Pathos and CRO Clinical Research Associates for day‑to‑day trial communications Coordinate with Clinical...Work at officeLocal area3 days per week
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