Regulatory Affairs Associate, Oncology Trials
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Summit Therapeutics Inc. is seeking an Associate of Regulatory Affairs to support day-to-day regulatory activities for assigned projects, including preparation and compilation of submissions for regulatory agencies and coordination of submission timelines. You will work under the Regulatory Affairs Lead, ensuring accurate trackers, and contributing to global regulatory submissions and strategic planning across clinical studies. #J-18808-Ljbffr Socket.dev
- Summit Therapeutics Inc. is a biopharmaceutical oncology company focused on improving quality of life and addressing unmet medical needs. The Associate of Regulatory Affairs will support day-to-day regulatory activities for assigned projects, including submissions, timelines...Suggested
$97k - $114k
...Inc. is a biopharmaceutical oncology company with a mission... ...presently approved by any regulatory authority other than China... ...Ireland. Overview of Role: The Associate of Regulatory Affairs will support the day-to-... ..., including clinical trial application (CTA) and IND...Suggested- Summit Therapeutics Inc. is seeking an Associate of Regulatory Affairs to support day-to-day regulatory activities for assigned projects, including CTA/IND submissions and health-authority interactions. The role involves coordinating submissions, maintaining timelines,...Suggested
$97k - $114k
...Inc. is a biopharmaceutical oncology company with a mission... ...presently approved by any regulatory authority other than China... .... Overview of Role: The Associate of Regulatory Affairs will support the day-to-day... ...activities, including clinical trial application (CTA) and IND...SuggestedContract workFor contractorsFor subcontractor- Summit Therapeutics Inc. is seeking an Associate of Regulatory Affairs to support day-to-day regulatory activities for assigned projects, including submissions to regulatory agencies and maintenance of submission timelines. The role involves coordinating with cross-functional...Suggested
- ...and Pain Medicine at Stanford Medicine is seeking a Clinical Trials Regulatory Specialist 1 to provide centralized regulatory support for a... ..., or experience working with anIRB. Knowledge of regulatory affairs, including FDA regulations, IRBreview and approval process, and...Local areaWorldwide
- Stanford Medicine's Department of Anesthesiology, Perioperative and Pain Medicine seeks a Clinical Trials Regulatory Specialist 1 to provide centralized regulatory support across a diverse clinical research portfolio. The role guides teams through HRPP/IRB processes and...
$186k - $233k
...Medicines is a late-stage clinical oncology company developing novel targeted... ...signaling pathway.The Opportunity:The Associate Director, Global Regulatory Affairs Project Management is an integral... ...with complex oncology clinical trial designs (e.g., combination studies...Full timeWork at officeLocal area- ...dashboards. Provides compliance advice to R&D and Tech Ops, identifying, mitigating, and managing fraud, abuse, kickback risks associated with clinical trials and other development activities; supports ethical decision‑making in clinical trial protocol, strategy, design, and...
$115.86k - $133.01k
...Transfer and Tangible Research property Agreements, draft language that complies with University, Federal and other sponsors and other regulatory policies, requirements, and conditions. Negotiate other research‑related agreements that involve intellectual property,...Hourly payFull timeContract workCasual workWork at officeRemote work$260k - $360k
...renowned interdisciplinary life sciences and healthcare regulatory practice seeks a mid-level associate to advise sophisticated provider, supplier, investor,... ...; annual retreats; practice-specific training; Trial School; deposition-skills workshops; and a proprietary...Work at officeLocal areaRemote workFlexible hours$135k - $185k
...of employment litigation matters from inception through resolution Manage pleadings, discovery, depositions, motion practice, and trial preparation Represent employer clients in administrative proceedings and related investigations Draft and argue substantive...Work at officeLocal areaRemote workFlexible hoursShift work$145k - $167k
...globally through transformational, accessible, clinically relevant diagnostic imaging. Learn MoreAbout The RoleJob Title: Senior Regulatory Affairs SpecialistLocation:Palo Alto, CA or Guilford, CT (Hybrid, 3 days/week)The Senior Regulatory Affairs Specialist advises...Work experience placementWork at officeWorldwideWork visaNight shiftWeekend work3 days per week$24 - $27.6 per hour
LE POSTE VOTRE PROFIL Licensed Beauty Advisor - Full Time Publiée le 03.08.2026 Sephora Retail Référence : 292578 Ajouter aux favoris Ouvrir Partager Localisation : Palo Alto, United States Type de contrat : Permanent Job Exp...Hourly payPermanent employmentFull timePart timeFlexible hoursShift workNight shiftWeekend work- ...Job Overview A law firm seeks a Healthcare Regulatory Associate in Palo Alto. This role offers the opportunity to work on health innovation, representing companies from pre-formation to capital markets, including public health tech companies. Duties Advise on healthcare...Flexible hours
$40 - $70 per hour
Title: Compliance Analyst Location: Remote US - Must be available in PST hours Duration: 12+ months Compensation: $40-70/hr Work Requirements: US Citizen, GC Holders or Authorized to Work in the U.S. About this Featured Opportunity...Local areaRemote workFlexible hours$120k - $150k
...Certificates, Waivers & COAs Partner closely with engineering and flight test teams to ensure compliance alignment early in design Regulatory Engagement Serve as primary Pivotal representative to: Aeronautical Authorities including FAA (and offices including AIR,...Work at officeLocal area- ...Our Client, an American Biotechnology company, is looking for a Regulatory Affairs Specialist 4 for their Sunnyvale, CA/Hybrid location. Responsibilities: Provide regulatory guidance to product teams, develop regulatory plans, and review and approve product...
$186k - $233k
...Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS... ...the RAS signaling pathway. The Opportunity: The Associate Director of Regulatory Affairs will provide regulatory leadership to clinical development...Full timeWork experience placementLocal area- ...incident reporting, and annual assessments Maintain and update FedRAMP authorization documentation, including SSP, CIS, CRM, and associated artifacts Lead internal and external audits for frameworks including FedRAMP (NIST 800-53), ISO 27001/27701, PCI-DSS, NIST 800-17...Remote workFlexible hours
$126k
...capture, process consistency, and develop compliance metrics Leads or supports maintaining a complete and accurate inventory of regulatory requirements, including identifying requirement owners, and mapping requirement to guidance documents, controls, and trainings...Work experience placementFlexible hours$55 - $60 per hour
...Job Title: Sr. Regulatory Affairs Specialist Location: Sunnyvale, CA, United States Type: Contract Compensation: $55.00 - $60.00 Work Model: Hybrid Overview Established Medical Device company is looking to hire a Sr. Regulatory Affairs...Contract workTemporary workLocal area- Veterans Health Administration is seeking an Equal Employment Opportunity Specialist to assist the EEO Manager in planning, development, implementation, evaluation, and monitoring of affirmative action and equal employment opportunity programs within the VA Palo Alto Health...
- BCG Attorney Search seeks a Healthcare Regulatory Associate in Palo Alto to counsel a leading health-tech focused law firm on regulatory matters, including HIPAA, Stark Law, and state privacy rules. The role involves advising companies from pre-formation through capital...Shift work
- ...internal stakeholders on tariff impacts and compliance requirements. Maintain compliant records and documentation in accordance with regulatory requirements. Ensure regulatory compliance by staying updated about changes to Customs laws and regulations, tariff measures,...
- A dynamic technology staffing firm is seeking an experienced Interim Trade Compliance Specialist in Palo Alto, CA, for a 6-month contract. The candidate will support international parts imports and facilitate compliance with customs regulations. This role requires strong...Contract workInterim role
$110k - $125k
...Compliance Specialist. This individual will serve as a critical stop‑gap, immediately alleviating the urgent operational workload associated with international parts imports and ensuring continuity until our full‑time Trade Compliance Manager is onboarded. This role...Full timeInterim roleImmediate start$55 - $60 per hour
Job Details Job Title: Regulatory Affairs Specialist IV Location: Sunnyvale, California Type: 6 month contract Compensation: $55-60/hour depending on qualifications Work Model: Hybrid - 3 days onsite Hours: 40.0 Overview Lead regulatory strategy and submissions for...Contract workLocal area$50 - $55 per hour
...for a 6‑month contract. This individual will serve as a critical stop‑gap, immediately alleviating the urgent operational workload associated with international parts imports and ensuring continuity until our full‑time Trade Compliance Manager is onboarded. This role...Full timeContract workTemporary workInterim roleLocal areaImmediate start$41.28 - $54.75 per hour
...and deviations from established policies and procedures to the Associate Director. Coordinates and integrates program compliance... ...levels of the organization. Knowledge of local, state and federal regulatory requirements related to areas of functional responsibility. Knowledge...Hourly payWork experience placementLocal areaImmediate start
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