Senior Clinical Research Associate, Sponsor Aligned, Oncology
$71.9k - $189kIQVIA
Job Overview Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking cancer research and make a real impact on patients’ lives. Key Responsibilities Site Monitoring Visits: Conduct selection, initiation, monitoring, and close-out visits in line with GCP and ICH guidelines. Subject Recruitment: Collaborate with sites to develop and track recruitment plans, ensuring project needs are met. Training & Communication: Provide protocol and study training to sites, maintaining regular communication to manage expectations and address issues. Quality Assurance: Assess site practices for protocol adherence and regulatory compliance, escalating quality issues as needed. Study Progress Management: Oversee regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution. Support start-up phases as required. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator’s Site File (ISF) per GCP/ICH and local regulations. Reporting: Generate visit reports, follow-up letters, and other necessary documentation. Mentorship: Mentor clinical staff through co-monitoring and training visits. Collaboration: Work closely with study team members to support project execution. Qualifications Education: BS degree required; a degree in a scientific discipline or healthcare is preferred. Experience: 3+ years of on site oncology monitoring experience strongly preferred. 1.5+ years of oncology monitoring experience can be considered. Phase 1 oncology experience is required. Skills: Proficient in GCP and ICH guidelines; Strong therapeutic and protocol knowledge in Phase 1 oncology trials; Excellent computer skills, including Microsoft Office and mobile devices; Effective communication, organizational, and problem‑solving abilities; Strong time management skills; Ability to build and maintain effective working relationships. Benefits Potential base pay range: $71,900.00 - $189,000.00. The actual base pay offered may vary based on job‑related qualifications, location, schedule, and other factors. Incentive plans, bonuses, and other compensation may be offered, in addition to a range of health and welfare benefits. Why Join Us? Be part of a team that’s pushing the boundaries of cancer research. You’ll have the opportunity to work on cutting‑edge Phase 1 oncology trials, collaborate with top professionals in the field, and contribute to life‑changing advancements in cancer treatment. If you’re passionate about making a difference and have the expertise we’re looking for, we’d love to hear from you! Equal Opportunity Employer IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. EEO: Minorities, Females, Protected Veterans, Disabled. #J-18808-Ljbffr IQVIA
$71.9k - $169.3k
...Clinical Research Associate, Sponsor Dedicated, IQVIA page is loaded## Clinical Research Associate, Sponsor Dedicated, IQVIAlocations: Overland Park... ...experience with expertise in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology. Candidates can be located anywhere in...SuggestedFull timePart timeLocal areaImmediate startWorldwide$69.8k - $226.8k
...Job Overview Join our team as a Clinical Research Site Manager, where you’ll play a crucial role... ...adhere to all protocols, regulations, and sponsor requirements. Essential Functions Site... ...experience, with a preference for oncology or immunology. Knowledge: In-depth understanding...SuggestedFull timePart timeLocal areaImmediate startWorldwide$101.6k - $169.3k
...IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH... ..., applicable regulations and guidelines, and sponsor requirements. Key Responsibilities Perform site...SeniorFull timePart timeLocal areaImmediate start- ...Clinical Research Associate Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study... ...protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring...SuggestedLocal area
$87.2k - $169.3k
...Senior CRA 1 IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal... ...seeking a dedicated Clinical Research Associate (CRA) to join our team... ...requirements, and sponsor expectations. Your work... ...monitoring, and close-out in alignment with the contracted scope...SeniorFull timePart timeImmediate startWorldwide$71.9k - $189k
IQVIA is looking for a Site Monitor in Overland Park, Kansas. The role involves site management and monitoring to ensure compliance with protocols and regulations. Candidates should have at least 2 years of monitoring experience and preferably a Bachelor's Degree in a ...Work at office- ...Experienced Clinical Research Associate - Sponsor Dedicated 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 to...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
$87.2k - $182k
IQVIA seeks a Monitoring Specialist in Overland Park, Kansas. This role involves performing monitoring and site management tasks to ensure compliance with study protocols and regulations. Candidates should have a Bachelor’s Degree in a scientific discipline or health care...$71.9k - $169.3k
IQVIA Argentina is hiring a Clinical Research Associate in Overland Park, Kansas. The role includes monitoring and managing clinical trial sites... ...experience in clinical research, particularly in fields like Oncology or Neurology, and possess a Bachelor’s degree in a...$78k - $130k
...French. Manage, deliver and/or perform full clinical site monitoring services for one or more... ...site budgets and regulatory filings that aligns with SOPs, study guidelines and GCP best... ...of site/patient issues or to address Sponsor concerns. May represent Director, Monitoring...SeniorRemote workWork from home$71.9k - $169.3k
IQVIA is seeking a Clinical Research Associate in Overland Park, KS to perform monitoring and site management. The role includes ensuring that sites comply with regulations and study protocols while managing site-related data. The ideal candidate should hold a Bachelor'...- A leading clinical research organization is seeking a Senior Clinical Research Associate 1 in Overland Park, Kansas. This role involves monitoring clinical study sites, ensuring compliance with protocols, and managing site relationships. The ideal candidate will have a...Senior
- A prominent healthcare organization is seeking a remote Clinical Research Associate (CRA) to manage clinical site monitoring services for various projects. The role requires fluency in both English and French, with a focus on site recruitment, oversight of project budgets...SeniorRemote work
- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to manage site activities focusing on regulatory and protocol compliance. The role requires a Bachelor's degree in a related field and strong communication skills, with responsibilities...SeniorRemote job
- A leading healthcare organization in Kansas City is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities ensuring compliance with protocols and quality standards. The ideal candidate will possess an advanced degree, extensive CRA experience...Senior
- Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions 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...SeniorFlexible hours
$96.2k - $151.4k
...throughout all phases of a clinical research study, taking overall responsibility... ...in compliance with ICH-GCP, Sponsor SOPs, Local Laws &... ...Protocol, Site Monitoring Plan and associated documents. Gains an in-... ...GCP), IT Change Management, Oncology, Pharmacovigilance, Policy...Full timeFor contractorsLocal areaRemote workRelocationVisa sponsorshipFlexible hoursShift work2 days per week3 days per week- IQVIA in Overland Park is looking for a Clinical Research Associate to join their dynamic team. This role involves monitoring and managing clinical... ...ideal candidate will hold a BS degree and have preferred oncology monitoring experience. Join us in making a real impact on...Senior
$200k - $235k
...is a biopharmaceutical oncology company focused on... ...strong business acumen, clinical expertise and market awareness... ...engagement plans in alignment with therapeutic area... ...development and research initiatives across development... ...investigator‑sponsored trials. Identify, gain...Senior- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating... ...requirements. Prepare for and attend investigator meetings, sponsor face‑to‑face meetings, global clinical monitoring/project...Interim roleLocal areaImmediate startRemote workFlexible hours
- ...Clinical Research Associate - California 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...Flexible hours
- A leading clinical research organization is seeking a Clinical Research Associate dedicated to supporting clinical trials. The ideal candidate should have 1-2 years of onsite monitoring experience, a bachelor's degree in a scientific discipline, and a strong understanding...
$101.6k - $169.3k
IQVIA Argentina in Overland Park is seeking a Site Manager to perform monitoring and site management tasks in clinical research. Ideal candidates should have a Bachelor's degree in a scientific or healthcare field and at least 2 years of on-site monitoring experience. This...- Join IQVIA, where we value integrity and diversity, and contribute to impactful clinical studies that enhance patient care. #J-18808-Ljbffr IQVIA
$47.4k - $169.3k
IQVIA Argentina is looking for a Clinical Research Associate in Overland Park, United States. This full-time position involves performing site monitoring and management to ensure compliance with study protocols and regulatory guidelines. The ideal candidate will have a...Full timeWork at office- Department:SOM KC Cancer Center Clinical Trials-Clinical ResearchPosition Title:Senior Laboratory Coordinator... ...for coordination of oncology clinical trial study... ...studies for Industry-Sponsored, Cooperative Group and... ...trials and world class research.Job Description:Job Duties...SeniorWork experience placementWork at office
- ...sciences and in the support of clinical studies. In over just 30... ...thrives working in cutting-edge research, fosters solid client... ...BioPharma Services team as a Senior Principal Investigator (SPI)/... ...analysis studies partnering with sponsors, toxicology and clinical...SeniorFull timeContract workWork experience placementWork at officeMonday to Friday
- ...leading technology services provider in Overland Park is seeking a Senior Product Lead to enhance product ownership and accountability... ...product vision, managing product backlogs, and ensuring outcomes align with business objectives. Ideal candidates have over 8 years of...Senior
- Pape-Dawson Engineers seeks an Associate Vice President of Public Works in Overland Park, KS to lead planning, design, and delivery of complex... .... You will guide cross-functional teams, mentor staff, and align efforts with company standards and strategic objectives. You...Senior
- The University of Kansas Medical Center is seeking a Senior Laboratory Coordinator to oversee oncology clinical trial specimens and supplies. This position requires coordination with various departments to ensure compliance with study protocols. Applicants should have...Senior
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