Associate I, Regulatory Affairs
Corcept Therapeutics
Corcept Therapeutics seeks a regulatory affairs associate to support clinical and nonclinical regulatory strategy development, health authority interactions, and global submissions for cortisol-modulating therapeutics. The hybrid role involves cross-functional collaboration to advance products through regulatory pathways.
Responsibilities
- Support preparation, review, and submission of regulatory documents and submissions
- Coordinate with clinical research organizations and health authorities on global submissions
- Assist in organizing briefing materials and responses for health authority meetings
- Track regulatory timelines, deliverables, and health authority commitments
- Collaborate with nonclinical and clinical teams to compile documents for regulatory filings
Requirements
- Bachelor's degree required; advanced degree in life sciences preferred
- Strong interpersonal and written communication abilities
- Ability to manage multiple assignments concurrently with attention to timelines
- Proactive problem-solving and adaptability to shifting priorities
- Experience working collaboratively within cross-functional teams
$186k - $233k
...act with urgency and hold ourselves to a high standard of rigor—all in service of patients.The Opportunity:The Associate Director, Global Regulatory Affairs Project Management is an integral part of the global Regulatory Affairs organization and is responsible for translating...SuggestedFull timeWork at officeLocal areaWorldwide- ...Revolution Medicines seeks an Associate Director of Global Regulatory Affairs Project Management to oversee submission timelines and execution plans for oncology drug development programs. This role translates regulatory strategies into actionable plans, coordinating cross...Suggested
$123.26k - $141.9k
...invoicing terms.Negotiate complex Material Transfer Agreements, draft language that complies with University, Federal and other regulatory policies, requirements and conditions.Negotiate other research-related agreements that involve intellectual property, publication...SuggestedContract workWork at office2 days per week$125.6k - $177.3k
...Corcept Therapeutics seeks a Senior Associate in Regulatory Operations to support regulatory submissions and compliance activities. The role involves managing electronic submissions to health authorities, maintaining regulatory systems, and collaborating across departments...Suggested- ...Corcept Therapeutics seeks an Associate Director of Regulatory Affairs to lead domestic and international regulatory strategy, submissions, and health authority interactions. The role involves coordinating cross-functional teams, maintaining compliance with regulatory...Suggested
$169.23k - $245.38k
...governance structure required to make the program audit-ready, banking-partner-ready, and scalable.The Director is accountable for regulatory interpretation, program-level risk assessment, sanctions governance, escalation standards, training substance, audit response,...- Job Description Job Description Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience...
$134k - $156k
...impact and change the world.The RoleThe a16z Compliance Team is looking for a Compliance Analyst to join their group and own the regulatory requirements related to the Firm’s core compliance needs. This individual will be a cross-functional contributor, working with employees...Work at office2 days per week- ...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,...
$145k - $175k
...periodic travel to Redwood City for team meetings, planning, and other business needs. Position Overview The Principal Regulatory Affairs Specialist drives the full spectrum of regulatory activities, from initial market authorization through post-market...Interim roleRemote work3 days per week$166k - $195k
...demonstrating integrity, accountability, equality and clarity across communications and decision making.Summary:The Sr. Project Manager, Regulatory CMC will serve as a key contributor to the company’s project management, regulatory and CMC functions. Reporting to the Vice...3 days per week$145k - $170k
Important: this position will work on the Weekend Shift team, with the following rotation schedules:Tuesday-to-Saturday (including Tue, Wed, Thur, Fri, and Sat), 9AM-to-5PM.Sunday-to-Thursday (including Sun, Mon, Tue, Wed, and Thur), 9AM-to-5PM.This position will rotate...Immediate startWorldwideShift workWeekend work$103.6k - $129.45k
LOCATION:This will be a hybrid role (1 day a week) working out of our San Carlos, CA location.POSITION SUMMARY: Natera is a global leader in cell-free DNA testing, supporting oncology, women’s health, and organ health. Our goal in R&D operations data science is to support...Immediate startWorldwide1 day per week$35 per hour
...lifecycles to ensure appropriate data access is established before work begins.Own the configuration, quality, and governance of metadata associated with a large-scale content library, including testing, auditing, and validation of metadata changes.Maintain the accuracy of...Contract workTemporary workRemote workWorldwide$211k - $250k
...sensitivity to sunlight and liver damage. Who You Are A regulatory affairs leader who owns global regulatory strategy and execution for... ...experience in the biotech or pharmaceutical industry for Associate Director; 8 years for Director, including experience leading...Flexible hours$25 - $35 per hour
...coordinates compliance processes, maintains accurate and audit-ready records, and helps ensure adherence to organizational policies, regulatory requirements, and BGCA standards. Reporting to the Senior Director of People Operations, with a dotted-line partnership to the...Full timeWork experience placementSeasonal workWork at officeLocal areaRemote workMonday to FridayShift workDay shift- ...Responsibilities: manage integrated launch schedules, oversee critical path milestones, coordinate cross-functional teams (Commercial, Medical, Regulatory, Supply, IT), track risks, and develop KPIs; support resource planning, process improvements, and dashboard maintenance....
$252k - $315k
...and team meetings.Specifically, you will be responsible for:Partner across the company including with clinical development, medical affairs, market access, to drive indication strategy, shape brand strategies across the product team.Ensure global readiness to drive...Full timeLocal areaRemote workWorldwide$226.19k - $292.71k
...pratices related to interactions between commercial, medical affairs and market access.Invest time and effort in building strong relationships... ....Recognize and assess healthcare compliance risks and develop associated mitigation controls to help address, as needed.Partner as...Full timeFor contractorsLocal area- # Program Manager, Compliance AssuranceMenlo Park, CA+2 locationsProgram Management+ 2 moreApply nowMeta's Regulatory Compliance Programs (RCP) is the central engine driving risk management and compliance at the company, supporting Meta and the family of apps. We're seeking...
$136k - $217k
...reviews, quality assurance checks, and provide constructive feedback and guidance to team members to ensure consistency, accuracy, and regulatory compliance across reviews. Qualifications5 years of relevant experience. Preferred Qualifications: 6 or more years of work...Full timeWork experience placementWork at officeLocal area$163k - $227k
The Regulatory Readiness Obligation Management team works across regulatory domains (e.g. AI, Privacy, Integrity, Security) and partners closely with Legal, Policy, Operations, and Product to understand and respond to key external pressures that could impact Meta's businesses...Hourly payLocal area$129.5k - $175k
...with internal teamsExecute external audits with third-party auditors and maintain relationshipsWork across multiple frameworks and regulatory standards, including but not limited to ISO, PCI, NIST, AICPA SOCDrive improvements in existing processes and develop new...Live inWork at officeShift work3 days per week$80.46 - $112.64 per hour
Chief Philanthropy Officer Inspired by faith. Driven by innovation. Powered by humankindness. CommonSpirit Health is building a healthier future for all through its integrated health services. As one of the nation's largest nonprofit Catholic healthcare organizations...Full timeLocal 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$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- ...sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: If you have difficulty...Permanent employmentTemporary workFor contractorsWork at officeLocal areaMonday to FridayShift workWeekday work
- ...EQ`s brand and reputation. Compliance aims to support the Board of Directors and Senior Management to fulfil their statutory and regulatory obligations, by helping to ensure compliance with the laws, regulations, principles and codes established by the regulator. What...Local areaWorldwide
- San Mateo County Sheriff's Activities League (SAL) seeks an Executive Director to oversee youth programs and partnerships with deputies and the community. The role leads program development, budgeting, fundraising, and policy implementation across county-wide initiatives...
- Natera seeks a Senior Data Analyst to design and build a next-generation AI-powered analytics platform for R&D operations. The hybrid role in San Carlos involves leveraging AI development tools while maintaining rigorous code quality and data accuracy standards. Responsibilities...Full time
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate I, Regulatory Affairs. Be the first to apply!
- regulatory contract Redwood City, CA
- regulatory engineer Redwood City, CA
- regulatory law Redwood City, CA
- clinical research regulatory Redwood City, CA
- regulatory cmc Redwood City, CA
- regulatory Redwood City, CA
- food regulatory Redwood City, CA
- regulatory technician Redwood City, CA
- regulatory scientist Redwood City, CA
- regulatory executive Redwood City, CA





