Own and manage the compliance program including SOC 2 and ISO 27001 readiness and audits.
Lead risk assessments, control testing, and enterprise risk management processes.
Partner with Engineering, Security, Product, Legal, HR, and Operations to embed compliance into business processes.
Calendly is a scheduling platform used by millions to automate meetings and streamline time management. They are a rapidly growing SaaS company fostering a culture of learning and high performance.
Manage day-to-day legal affairs for Life Sciences/Pharma companies, advising on regulatory risks and negotiating commercial contracts.
Draft, review, and negotiate various agreements including customer, distributor, vendor, and quality agreements.
Champion process improvements, provide training on legal topics, and support corporate and litigation matters.
FUJIFILM Holdings America Corporation redefines innovation across healthcare, photography, semiconductors, and data storage, leading 23 diverse affiliate businesses in the Americas. With over 70,000 employees globally across four key business segments, the company offers a flexible work environment and a culture where innovation thrives.
Execute regulatory strategies for obtaining registration approval of Intuitive's medical device portfolio in APAC indirect markets.
Coordinate with Distributor RAs and internal stakeholders to compile regulatory documentation and ensure compliance with medical device regulations.
Manage regulatory submission tracking in systems like Veeva and perform periodic surveillance activities using TrackWise.
Intuitive is a pioneer and market leader in robotic-assisted surgery, dedicated to advancing minimally invasive care. The company has built an inclusive and diverse team of great people for over 25 years, grounded in integrity and a strong capacity to learn.
Advise on payments products and infrastructure, including payment rails, product launches, and operational incidents.
Partner across Product, Compliance, Risk, Engineering, and Legal to bring legal perspective early.
Help launch new payment capabilities like Zelle, navigating regulatory complexity.
Mercury is a fintech company on a mission to reinvent banking for the modern age. The company blends design and technology to offer banking and financial products, and is known for its culture of urgency and curiosity.
Draft, negotiate, and manage a wide range of commercial, clinical, and operational agreements.
Partner with internal stakeholders to assess legal risks and facilitate successful business outcomes.
Drive continuous improvement of contracting processes, templates, and systems.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines for hypertension and related comorbidities. As a fully remote pre-commercial biotech, we value collaboration and innovation in a fast-paced environment.
Build and mature a best-in-class compliance program aligned with OIG guidance and industry standards.
Draft, implement, and refresh compliance policies, training, and monitoring initiatives.
Manage HCP engagement programs, including FMV assessment and regulatory compliance.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. It is headquartered in Radnor, Pennsylvania, and operates as a fully remote company.
Own Convergent's legal strategy, set the overall risk framework, and advise senior leadership on significant decisions.
Lead IP strategy, manage outside counsel, and develop playbooks that empower teams to make deliberate IP decisions.
Manage the legal team, ensure 501(c)(3) compliance across the portfolio, and navigate international regulatory complexity.
Convergent Research is a non-profit science studio that pioneers Focused Research Organizations (FROs) to remove bottlenecks in breakthrough scientific research. The organization has grown to 200 people with a $100M annual spend, operating 13 subsidiary FROs, and values agility, creativity, and risk tolerance.
Review, draft, negotiate, and track legal agreements including confidentiality agreements, clinical study agreements, and amendment agreements across APAC.
Set up contracting strategies for assigned projects and work closely with Clinical Operations study team to ensure deliverables align with study timelines.
Be fully responsible for Site Contract Management from setting up site contracting strategy to execution of contracts, including budget negotiations with sites.
Precision for Medicine is a CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients. They have brought together new technologies, expertise, and operational scale to help the life sciences industry.
Manage regulatory relationships by coordinating communications and preparing materials for authorities.
Draft and review regulatory correspondence while supporting governance activities and risk assessments.
Track legislative changes and assist with compliance training, reporting, and cross-functional projects.
Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. They use technology to streamline recruitment and focus on fair, objective candidate evaluation.
Drive regulatory strategies for Expanded Access Programs across global markets, ensuring compliance and patient access.
Act as a subject matter expert in communications with pharmaceutical clients, health authorities, and cross-functional teams.
Prepare and submit regulatory dossiers while maintaining up-to-date knowledge of global frameworks.
Jobgether uses AI-powered matching to connect candidates with jobs at partner companies. They are a fast-growing global organization with a dynamic scale-up environment and high autonomy.