Clinical Research Associate [Remote]
ICON plc
- Remote job
Clinical Research Associate, Onc/Hem
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 analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
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 1 year 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%)
- Must be located in PA, NY, NJ, MA, ME, VT, NH, CT, RI
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
$91.34k - $114.17k
Clinical Research Associate, Onc/Hem 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...SuggestedWorldwide- Experienced Clinical Research Associate | Regionally Aligned Across US 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...SuggestedFull timeContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- The Clinical Research Associate (CRA) has local responsibility for the delivery of studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/Local Study Associate Director...SuggestedHourly payTemporary workLocal areaRemote workFlexible hours
$74.5k - $197.5k
...Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) IQVIA is actively seeking experienced Clinical Research Associates II (CRA II) and Senior Clinical Research Associates (Sr. CRA) to support a range of clinical studies across multiple...SuggestedFull timePart timeWork at officeImmediate startWorldwide$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...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...
$125k - $142k
...WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants... ...trials and respond to emergency situations based upon clinical research standards. Responsibilities : Responsible for all aspects...Full timeWork at officeLocal areaRemote workNight shift$92.32k - $126.94k
...that drive clear economic value, better clinical outcomes and improved quality of life for... ...CRA supports the day to day operations associated with the execution of clinical trials. He... ...of operational aspects of clinical research and regulatory regulations; Good interpersonal...Temporary workWork experience placementInterim roleWorldwide- ...Clinical Research Monitor Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Perform site monitoring...Local area
$140k - $145k
...Senior Clinical Research Associate Location: San Jose/San Francisco, CA Type: Embedded Salaried Contract Compensation: $140,000.00 - $145,000.00 Work Model: Remote with Regional Travel Hours: 40.0 hours/week We are looking for a Senior Clinical Research Associate...Contract workZero hours contractLocal areaRemote workWork from home- A software development company seeks a Clinical Research Associate in Raritan, NJ. The ideal candidate will have at least 5 years of site management experience, including 2 years in field monitoring. Strong communication, planning, and interpersonal skills are necessary...
$129k - $203.1k
...primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.... ...Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study protocol...Remote jobFor contractorsLocal area2 days per week3 days per week$142.4k - $224.1k
...role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director or Head of Site Management and... ...responsible to manage a team of 6-14 Clinical Research Associates (CRAs) and to ensure excellent study and site performance...Remote jobFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$64k - $189k
...IQVIA seeks an experienced Clinical Research Associate for sponsor-dedicated monitoring and site management across multiple U.S. regions. The role involves conducting site visits, managing study progress, ensuring regulatory compliance, and supporting recruitment and enrollment...$74.5k - $197.5k
...Clinical Research Associate role supporting sponsor-dedicated monitoring activities across multiple U.S. sites. Responsible for site management, protocol compliance, data integrity oversight, and regulatory documentation in accordance with GCP and ICH guidelines. Responsibilities...Work at office- ...Note- this contract is 100% onsite so please only submit local candidates to the below address in WI. Title – Clinical Research Coordinator Number of Leased Workers needed – 1 Tentative start date – asap Tentative end date – 12 months...Permanent employmentContract workTemporary workWork at officeLocal areaImmediate startShift workDay shift
$87.2k - $182k
...Clinical Research Associate supporting sponsor-dedicated clinical trials across multiple U.S. locations. Responsibilities include site monitoring, protocol training, recruitment tracking, data quality oversight, and regulatory documentation management to ensure protocol...Work at office$78k - $98k
...Our client, a pharmaceutical company based in Morristown, New Jersey, is hiring a Clinical Research Associate to oversee clinical trial activities across multiple study sites. This role involves monitoring site compliance, verifying data integrity, and ensuring adherence...Full timeInterim roleWork at office- ...Description Description: SUMMARY: Zydus Therapeutics is a clinical stage, specialty-focused bio-pharmaceutical company focused on... ...of Zydus Lifesciences, our pipeline is fueled by 1,300 researchers who are working with cutting-edge technologies to discover new...Work at officeLocal areaRemote work
$75k - $90k
ABOUT VITALIEF Vitalief is a clinical research consulting firm focused exclusively on the clinical research industry, providing consulting, staffing, and technology-enabled services to academic medical centers, health systems, sponsors, CROs, and site networks. By combining...Full timeTemporary workWork at officeLocal area- Canfield Scientific, Inc. is seeking a Clinical Project Associate who can prioritize, multitask, and communicate clearly in a fast-paced environment. The role supports designated clinical project teams with quality, timelines, and project specifications, and involves document...Work at office
$23 - $28 per hour
An ideal candidate for our Clinical Project Associate position is an individual who can prioritize and multitask, is experienced in windows-based computer applications, and possesses strong communication skills. The right individual will have strong time management skills...Hourly payWork experience placementWork at officeFlexible hoursShift work- Canfield Scientific, Inc. in New Jersey is seeking a Clinical Project Associate to provide project management and operational support for designated clinical projects. You will help manage documentation, coordinate shipments, and support data queries to ensure timelines...Work at officeShift work
- Canfield Scientific, Inc. is seeking a Clinical Project Associate in Parsippany, New Jersey. The role involves coordinating clinical project activities, maintaining study documentation, and supporting data management to ensure timely, high-quality study deliverables. The...Hourly payWork at office
- Canfield Scientific, Inc. is seeking a Clinical Services: Clinical Project Associate to provide project management and operational support to designated clinical project teams, ensuring quality, timelines, and specifications are met. The role involves document management...Work at office
$74.5k - $197.5k
...IQVIA seeks experienced Clinical Research Associates II and Senior Clinical Research Associates to oversee clinical trial sites across multiple therapeutic areas nationwide. The role involves managing all phases of site monitoring, ensuring protocol compliance, regulatory...Work at office- ...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...Contract workWork at officeLocal areaFlexible hoursAfternoon shift
- Canfield Scientific, Inc. is seeking a Clinical Project Associate to provide project management and operational support for designated clinical projects. The role involves ensuring quality, timelines, and project specifications are met, while aiding in documentation and...Work at office
- Canfield Scientific, Inc. in New Jersey is seeking a Clinical Projects Associate to support clinical project teams with documentation, data management, and timely execution of study activities. The role emphasizes multitasking, strong communication, and proficiency in Windows...Work at office
- Canfield Scientific, Inc. in Parsippany, New Jersey, is seeking a Clinical Projects Associate to provide project management and operational support to designated clinical project teams, ensuring quality, timelines, and project specifications are met. The role involves managing...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Associate [Remote]. Be the first to apply!
- clinical research administrator New Jersey
- clinical trials assistant New Jersey
- on-site clinical research associate (traveling/remote) New Jersey
- clinical research assistant New Jersey
- clinical research associate New Jersey
- senior devops engineer remote New Jersey
- clinical research remote New Jersey
- remote support technician New Jersey
- remote qa New Jersey
- remote senior project manager New Jersey

