Senior Clinical Research Associate [Remote]
$110.52k - $138.15kIcon Clinical Research
- Remote job
Senior Clinical Research Associate - Oncology - New York
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.
Responsibilities:
Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness
Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites
Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials
May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs
Promptly document monitoring activities and submit/approve visit reports
Manage site essential document collection and TMF reconciliation with site files
Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals
Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution
Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans
Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations
Support sites and the client's regulatory inspections
Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities
Lead site engagement initiatives and foster relationships with key Oncology sites and networks
Qualifications
Bachelor’s degree (scientific field preferred)
5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.
1+ years early development trial experience
Solid tumor clinical trial experience is required
Experience utilizing Veeva systems is highly preferred
Demonstrated experience developing/maintaining site relationships and securing compliance
Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology
Experience collaborating with sites from initial engagement through close-out phases
Experience activating sites
Experience training site staff
Experience supporting sites and/or sponsors in regulatory inspections
Experience working within a Functional Services (or in-house) monitoring model is preferred
Willing to travel up to 50%
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.
Salary range: $110,520.00-$138,150.00
Bonus, Com, Stock, Benefits & Disclaimer verbiage:
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
Are you a current ICON Employee? Please click here to apply
- ...Our Client is a rapidly growing international Clinical Research Organisation offering an experienced( Senior ) CRA opportunity to work from home on full FTE as part of their team in Italy . Responsibilities: Conducting start-up activities and monitoring visits Maintaining...SeniorWork from home
- ...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...SeniorInterim role
- ...Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long-term engagement in the US with one of our Global Medical Device... ...including holiday, vacation, and sick/personal time. Senior Clinical Research Associate Travel up to 75% To...SeniorFull time
- ...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 study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local...SeniorLocal areaRemote workFlexible hoursShift work
$38 - $40 per hour
...the job poster from Baim Institute for Clinical Research Director, Human Resources at Baim... ...Clinical Research The Sr. Clinical Research Associate/Field Monitor Contractor performs... ...is dependent on study specific needs. Seniority level Seniority level Mid-Senior level...SeniorPart timeFor contractorsInterim roleRemote workWork from home10 hours per week$120k - $135k
...more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most... ...on patients globally.Role Overview:We are seeking a Senior Clinical Research Associate (CRA) to support our Clinical Operations team. The Senior...SeniorTemporary workWork at officeImmediate startVisa sponsorship$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...SeniorFull timeWork at officeImmediate startRemote workWork visa3 days per week$103k - $130k
...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... ...possible. The Sr. Clinical Research Associate (Sr. CRA) is responsible for?set-up,...SeniorHourly payContract workRemote workWork from homeWorldwideFlexible hoursNight shift$103k - $130k
...Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate (Sr. CRA) is responsible for the set‑up, initiation, execution, monitoring and close‑out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The...SeniorContract workRemote workNight shift$101.6k - $169.3k
...Senior Clinical Research Associate 1 IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory: Job Overview: Perform monitoring...SeniorFull timePart timeLocal areaImmediate startWorldwide- ...Senior CRA / CRA II - Home-Based (US) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation... ...experience as a Clinical Research Associate, with a strong understanding of...SeniorRemote jobWork from homeFlexible hours
- ...Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect... ...variety of therapeutic indications. Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and...Contract workWork visa
- ...Clinical Research Associate II Remote, Poland Precision for Medicine, Oncology and Rare Disease is not your typical CRO. We are passionate... ...commitment (international travel may be required for some senior level positions) Fluency in English and for non-English...Local 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$65k - $75k
...Clinical Research Associate - Central U.S. Remote The Clinical Research Associate (CRA) role focuses on supporting clinical trials, regulatory... ...colleagues. Networking skills and the confidence to interact with senior experts, orthopaedic, and neurological surgeons. Critical...Work at officeLocal areaImmediate startRemote work- ...A leading healthcare institution is seeking a Research Associate in New York City. This position involves conducting independent basic science experiments and collecting clinical data, with a focus on training new staff in research methodologies. Candidates must have...Daily paidFlexible hoursAfternoon shiftEarly shift
- ...Clinical Research Associate - Early Development Multi Therapeutic - Midwest Region ICON 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...Local areaRemote workVisa sponsorship
$91.34k - $114.17k
...Clinical Research Associate - Multi Therapeutic Area (Early Development) - 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...Work experience placementLocal areaVisa sponsorshipFlexible hours- ...Clinical Research Associate II When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution...Remote workFlexible hours
- ...Clinical Research Associate 1 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...Flexible hours
- ...Overview 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...Remote work
$96.2k - $151.4k
...through all phases of the trial. Performs clinical study site management/monitoring... ...Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth... ...closely with them to develop strong clinical research capabilities. Travel Requirements Ability...For contractorsLocal areaRemote workRelocationVisa sponsorshipFlexible hoursShift work2 days per week3 days per week$96.2k - $151.4k
...primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.... ...laws and regulations, protocol, site monitoring plan and associated documents. Gain an in-depth understanding of the study protocol...For contractorsLocal areaRemote workRelocationVisa sponsorshipFlexible hours2 days per week3 days per week$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- ...Clinical Research Associate II (FSP - Sponsor Dedicated) ICON 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, collaboration,...Remote work
- ...Clinical Research Associate The Clinical Research Associate 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...Local areaRemote workWeekend work
- ...Parexel Clinical Trial Management When our values align, there's no limit to what we can achieve. At Parexel, we all share the same... ...Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology...Local areaImmediate startRemote workFlexible hours
- ...Clinical Research Associate 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...
$58.66k - $81.68k
...Job Description 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-marketing studies...TraineeshipLocal area$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry... ...clinical monitoring experience, aligned to CRA II or Senior CRA I level. Experience supporting clinical trials within...Permanent employmentRemote work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Clinical Research Associate [Remote]. Be the first to apply!
- clinical research associate contract New York, NY
- clinical research administrator New York, NY
- clinical trials assistant New York, NY
- clinical research assistant New York, NY
- regional clinical research associate New York, NY
- clinical research associate cra New York, NY
- clinical research associate New York, NY
- senior clinical research associate New York, NY
- clinical research associate work from home New York, NY
- on-site clinical research associate (traveling/remote) New York, NY

