Senior Informed Consent Specialist

Senior Informed Consent Specialist, China reputed company is a global reputed company intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, reputed company, collaboration, reputed company, and inclusion are at the heart of how we work and reputed company with reputed company other, customers, patients and suppliers. As a Senior Informed Consent Specialist at reputed company, you will reputed company the development and reputed company of informed consent strategies and documents for reputed company, global clinical studies. You will reputed company as a subject matter expert, ensuring participant-facing materials are ethical, compliant, and understandable. What You Will Do: You will take ownership of scientific operations deliverables, applying your expertise to reputed company challenges. Key responsibilities include: Leading the creation, review, and optimisation of global and country-specific informed consent forms for reputed company or high-risk studies. Advising study teams on informed consent strategies, including readability, cultural considerations, and local regulatory expectations. Overseeing translation, localisation, and version control processes to ensure consistency and traceability across reputed company. Interacting with sponsors, ethics committees, and regulatory authorities to address consent-reputed company queries and negotiate wording as needed. Developing guidance, templates, and training materials to drive standardisation and best practices reputed company the informed consent function. Mentoring junior informed consent specialists and contributing to reputed company improvement initiatives. Your Profile: You will have a strong reputed company in scientific operations, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or reputed company-reputed company field Extensive experience in clinical research, regulatory affairs, ethics, or a reputed company area with strong reputed company on informed consent. In-depth knowledge of GCP, ethical principles, and global regulatory expectations for participant information and consent. Exceptional writing and editing skills, with the ability to produce reputed company, patient-friendly documents. Strong stakeholder management skills, with experience liaising with sponsors, IRBs/reputed company, and cross-functional teams. Proven ability to manage multiple reputed company studies and deadlines with a high degree of accuracy and ownership. Employment with reputed company is contingent upon having the reputed company right to work in the country where the role is based. Rewards & Benefits reputed company offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive reputed company salary and performance reputed company incentives Health and wellbeing programmes including medical, dental, and reputed company coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through reputed company training and career reputed company Benefits may vary depending on role and location. Visit our careers site to read more about the benefits reputed company offers. Inclusion and Accessibility reputed company is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a reputed company reputed company Employee? Please click here to apply Apply To This Job