
Manager, International Privacy
- London
- Permanent
- Full-time
- Assisting the Global Privacy Lead for GCO in providing support and (where appropriate) taking the lead on clinical trial-related privacy matters, including conducting privacy assessments on new business processes, handling escalations and questions related to informed consent forms and clinical trial agreements, and (where needed and under the instruction of Legal or Privacy) handling legal questions in informed consent forms and other related projects that may arise.
- Assisting with contractual matters related to data protection, such as data processing agreements, data transfer agreements (e.g. standard contractual clauses), etc. including the development and maintenance of templates.
- Working with the Privacy Office and Third-Party Risk Management to review questionnaires related to the due diligence of vendors’ data protection and security practices.
- Supporting the intake, evaluation of and response to data subject requests (e.g., request for information, clarifications, rectification or deletion of personal data) and reports of potential data incidents.
- Cross-functional projects under the direction of the Privacy Office or Legal that may arise, including those related to data transfers, privacy notices and consents, privacy assessments, cookie compliance, and training.
- Undertaking research to keep up-to-date with data protection developments affecting clients in the International region, as well as our GCO space, and anticipating potential changes needed to meet new regulatory requirements.
- Participating in various Legal & Compliance Department projects and initiatives (e.g., Culture, Diversity, & Inclusion Committee, Pro Bono & Community Engagement Committee, Talent & Development Committee, etc.).
- Bachelor’s degree or higher in a related field such as law or technology.
- CIPP/E, CIPM, CIPT certification(s) or equivalent preferred.
- Minimum of 3 years’ experience providing data protection advice, preferably to pharmaceutical, biotechnology, medical device, CRO or healthcare companies, whether in-house or at a law firm.
- Demonstrated knowledge and expertise required in GDPR. Familiarity with other data protection laws and regulations preferred.
- Experience and knowledge of data protection laws and regulations as they relate to research activities (e.g. clinical trials) preferred.
- Experience in OneTrust preferred.
- Demonstrated teamwork and collaboration skills, in particular providing support to global and multi-functional teams.
- Strong analytical and communication skills, with the ability to develop and deliver clear and concise information to a variety of stakeholders, both orally and in writing.
- Highly motivated to contribute and grow within a complex area of emerging importance.
- Ability to multi-task and handle multiple assignments in a fast-paced, deadline driven environment.
- Demonstrated experience of taking ownership and providing timely, actionable advice.
- Detail and solution oriented.
- Hybrid: work remotely up to two days per week; or select
- On-Site: work five days per week on-site with ad hoc flexibility.
We are sorry but this recruiter does not accept applications from abroad.