Oncology Clinical Research Regulatory Lead
Jefferson Health
Jefferson Health is seeking a Clinical Research Regulatory Coordinator to support oncology studies at the Sidney Kimmel Comprehensive Cancer Center. You will manage regulatory binders, coordinate PRI/IRB submissions, and ensure ongoing compliance with GCP and sponsor requirements. Reporting to a Regulatory Manager within the Clinical Trials Office, you will prepare amendments, continuing reviews, and regulatory documents for PRMC and IRB reviews, while assisting in staff training and workflow #J-18808-Ljbffr Jefferson Health
- ...on work experience in clinical data management within... ...clinical trial processes, regulatory requirements (GCP, ICH... ...of 3+ years of lead or project management... ...Job function Other and Research Industries Pharmaceutical... ...Clinical Data Manager-(Oncology) Remote Associate...Regulatory16 hoursFull timeWork experience placementWork at officeRemote work
- Worldwide Clinical Trials is seeking a Senior Site Activation Manager II to lead the start-up and activation of clinical research sites across complex studies. You will coordinate with sponsors, project teams, regulatory stakeholders, and sites to ensure readiness, compliance...RegulatoryRemote jobWorldwide
- Syneos Health/ inVentiv Health Commercial LLC is seeking a Clinical Research Associate to perform critical site management and monitoring activities, ensuring compliance with regulatory standards. This role requires a Bachelor's degree or RN in a relevant field, combined...RegulatoryFlexible hours
- ...Surgery at Maimonides Medical Center is seeking a full-time Clinical Research Coordinator to help build and run our growing research and education... ...will manage clinical trials from start to finish, oversee regulatory lifecycles (IRB submissions, continuing reviews), #J-18808-...RegulatoryFull time
$116k - $182.27k
...and empower you to shine? Join us as a Lead Clinical Study Manager based remotely reporting... ...ready” at all time; may be involved in regulatory inspections by preparing for and/or attending... ...industry and/or clinical research organization, including 4+ years clinical...RegulatoryMinimum wageFull timeContract workInterim roleLocal areaRemote workNight shift- Parexel is seeking a Clinical Research Associate II to manage sites across the United States in all study phases. You will serve as the primary... ...protocol adherence, data integrity, patient safety, and regulatory compliance while coordinating with sponsor teams. Ideal...Regulatory
$120k - $135k
...Companies is seeking an experienced Clinical Research Associate (CRA) to join our client’s... ...This opportunity is with an industry-leading Oncology Clinical Research organization supporting... ...trials, ensuring compliance with regulatory requirements, and maintaining high standards...RegulatoryRemote work2 days per week3 days per week- UBC in the United States is seeking a Lead Clinical Research Associate to provide clinical project oversight and support to the project management... ...team members, coordinate sponsor and PM meetings, manage regulatory submissions, and ensure audit-ready systems such as eTMF...RegulatoryRemote job
- ...process. Goodman Dermatology - Lead Medical Assistant -... ...surgery, vein care, and radiation oncology. Our team is seeking a Lead Medical... ...ensuring compliance with all regulatory standards, company policies,... ...point person for day-to-day clinical operations. They work...RegulatoryFull timeTemporary workWork at office
$135k - $159k
...owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded... ...excellence. ABOUT THE JOB The Lead Clinical Research Associate (LCRA... ...required by applicable law or regulatory requirements, ProTrials will...RegulatoryContract workInterim roleRemote workFlexible hours- The Sr. CRA at Terumo Medical Corporation supports day-to-day operations of clinical trials, monitoring multiple sites to ensure data quality, adherence to protocol, GCP, and regulatory requirements. Serving as the primary site liaison, you will train sites, collect regulatory...Regulatory
$170k - $200k
...sciences companies design optimal clinical trials. Our AI-powered... ...and outcomes. Faro empowers researchers to design more intelligent trials... ...Summary We are hiring a Lead Clinical Scientist to serve as... ...they reflect scientific rigor, regulatory awareness, and user-centric design...RegulatoryTemporary workWork at officeRemote workWork from homeFlexible hours$160.8k - $221.1k
...more modern, connected oncology ecosystem. We’re looking for a Lead Product Manager to help... ...impact on cancer care and research. You will own the end to... ...3 teams supporting core clinical workflows across Flatiron... ..., operations, and regulatory professionals You have a...RegulatoryWork at officeWork from homeFlexible hours- Lead Clinical Research Associate UBC / EDS / CRA - WPK Regular Research & Clinical Remote, US As a pharmaceutical support industry leader ,... ...Authority (CA), Central and Local Ethics Committee and other regulatory applications, as per country requirements May include...RegulatoryContract workTemporary workWork at officeLocal areaRemote workFlexible hours
$160.5k - $305k
...areas including immunology, oncology and neuroscience - and... ...that the Director leads by example and retains first-hand clinical insight that strengthens... ...medical personnel: Clinical Research Manager, Clinical Operations... ..., payers and Local Regulatory Authorities. AUTHORITY...RegulatoryFull timeLocal area$113 per hour
...confidential client is seeking a Study Lead Statistician (SLS) to lead... ...for product‑facing clinical studies. The SLS works cross‑... ...success, and compliant with regulatory standards and company procedures... ...pharmaceutical, biotechnology, or medical research environment. Strong...RegulatoryRemote workMonday to Friday- ...Chief Physician Assistant in the Bronx leads the Phase 1 oncology clinical trials program at Montefiore... ...studies. This role supervises APPs and research staff, manages the trial portfolio... ...sponsor relationships, and ensures regulatory compliance, quality, and efficient...Regulatory
- Parexel is expanding its Clinical Research Hub and seeks an Initiation Clinical Research Associate (iCRA) to join our team... ...line-manager support and a connected team. You will lead start-up activities, manage regulatory submissions, site activation, and protocol amendments...RegulatoryRemote jobWork from homeFlexible hours
- ...About this position The Senior Clinical Trial Leader Oncology acts as the face of Alentis towards external... ...Operations and/or Clinical Science lead and the face of Alentis towards external... ...budget quality standards and regulatory requirements. Provide strategic leadership...RegulatoryContract work
$68k - $120.5k
...Specialty and Payer Management, the Clinical Reviewer is a non-patient-... ...meet coverage criteria and regulatory standards. The Clinical... ...medications, infusion therapies, oncology, or high-cost treatment... ...Compensation Grade Clinical & Research Compensation Grade Profile Registered...RegulatoryFull timeWork at officeRemote work- ...the United Kingdom is hiring a Senior Clinical Research Associate/CRA II for a fully home-based... ...while contributing to high-quality oncology trials and benefiting from a collaborative... ...and ICH-GCP standards, and coordinate regulatory submissions, initiation visits, and...RegulatoryRemote workWork from home
- ...We are partnering with a leading life sciences organisation to recruit multiple Lead Clinical Data Managers to support clinical trials across the full study lifecycle... ..., ensuring high-quality data delivery, regulatory compliance and inspection readiness from study...RegulatoryRemote work
- Director, Clinical Research Operations Transformation ABOUT VITALIEF Vitalief... ..., focusing on Non‑Oncology programs and enhancing cross... ...coordination. A central focus will be leading the operational build‑out... ...optimization, IRB processes, and regulatory compliance. Experience with...RegulatoryFull timeTemporary workFlexible hours2 days per week3 days per week
- Precision for Medicine is a clinical research organization that combines novel trial designs,... ...with reasonable travel as required and oncology experience preferred. You will monitor... ...for protocol adherence and coordinate regulatory submissions and visits to ensure high-...RegulatoryRemote jobWork from home
- Precision for Medicine is seeking a Clinical Research Associate II / Senior CRA. This fully home... ...adherence to protocol, ICH-GCP, and regulatory standards, and support site setup and... ...+ years CRA experience in CRO/pharma, oncology experience, and English fluency. #J-1...RegulatoryRemote jobWork from home
- ...Thermo Fisher Scientific, is a leading provider of endpoint technology solutions for clinical trials. We are seeking a... ...Oncologist to support oncology-focused clinical research by providing expert medical... ...internal teams, sponsors, and regulatory stakeholders to ensure...RegulatoryWorldwideFlexible hours
- ICON is a global healthcare intelligence and clinical research organization seeking a Principal Scientist to lead scientific research and development programs. You will collaborate across clinical, regulatory, and data science teams, guiding study design, interpretation...Regulatory
- Mount Sinai Hospital is seeking a Clinical Trials Manager to oversee the STEP thrombectomy platform trial nationwide, coordinating performance... ...ability to drive study milestones, manage budgets, timelines, regulatory compliance, and develop training materials for site staff...Regulatory
$75.28k - $100k
...Hiring Department Medical Research Office Job Description This position provides nursing management and coordination of oncology clinical trials and research participants within the Clinical... ...activities. Participate in IRB and regulatory activities for assigned studies,...RegulatoryTemporary workWork at officeShift work$66.2k - $90k
...Description A Clinical Research Coordinator (CRC) II position is currently available within... ...compliance with institutional and national regulatory requirements Report adverse events... ...~2 years of clinical research ~ Oncology experience preferred Equal Opportunity...RegulatoryTraineeshipWork at officeLocal area
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