Senior Manager, Clinical Trial Disclosure and Transparency

Alnylam; EE. UU.; Presencial; USD 120.000 - 180.000; Jornada completa

Descripción de la vacante

Alnylam seeks a Senior Manager, Clinical Trial Disclosure and Transparency to lead the CTDT operations ensuring timely disclosure of trial information to regulatory bodies and public registries.

The role collaborates across Clinical Operations, Regulatory Affairs, Medical Affairs, Data Sciences and external stakeholders, shaping global disclosure strategies and maintaining compliant documentation while advancing AI initiatives in registration and results posting.

Formación

• Bachelor's degree in Life Science or English/Communications; advanced degree preferred.
• 6+ years in Clinical Trial Disclosure and Transparency in sponsor or CRO settings.
• Expert understanding of global regulatory requirements for clinical trial disclosure.
• Familiarity with ClinicalTrials.gov, EU CTIS and related registries.
• Detail-oriented with strong communication skills; able to work in global teams.
• Proficiency with Office apps and AI tools for disclosure workflows.

Responsabilidades

• Ensure accurate, timely, consistent, and complete disclosure of clinical trial data in line with regulatory requirements.
• Serve as subject matter expert for CTDT registration and results regulations.
• Plan and prepare protocol registration and results records for public registries; maintain records per regulation.
• Facilitate review and finalization of protocol and results content with stakeholders.
• Collaborate across Clinical Operations, Regulatory Affairs, Medical Affairs, Data Sciences and external partners; provide guidance on disclosure standards.
• Oversee interns, contractors, or training of junior CTDT team members.
• Act as super-user for disclosure/ transparency tracking, logging, and authoring tools.
• Support AI projects for registration and results posting workflows.
• Contribute to training manuals, SOPs, and process improvement initiatives.
• Represent CTDT on project teams and collaborative initiatives.

Conocimientos

Regulatory knowledge

Clinical trial disclosure

Global regulatory compliance

Project management

Communication

AI tools (CoPilot)

Educación

Bachelor's degree in Life Science or English/Communications

Herramientas

ClinicalTrials.gov

Microsoft Office

AI tools

Descripción del empleo

The Senior Manager, Clinical Trial Disclosure and Transparency is a key member of the Clinical Trial Disclosure and Transparency (CTDT) team working within the Alnylam Medical Writing Expertise Area. The Senior Manager, CTDT is responsible for expertly carrying out operations for the accurate and timely disclosure of Alnylam trial information to regulatory agencies and publicly accessible clinical trial registry websites.

Responsibilities

• Ensure accurate, timely, consistent, and complete disclosure of clinical trial data in alignment with global, regional, and local regulatory requirements.
• Serve as subject matter expert for CTDT registration and results regulations and
• Independently plan and prepare protocol registration and results records for public registries according to current guidelines and Alnylam policy, producing high quality and on-time writing deliverables; maintain records as per regulation.
• Facilitate/manage efficient review and finalization process for all protocol and results record content with key stakeholders.
• Collaborate effectively with all stakeholders including Clinical Operations, Clinical Development, Regulatory Affairs, Pre-Clinical Development, Program Management, Research, Medical Affairs, Safety, Quality, and Corporate Communications, Data Sciences as well as with external stakeholders, bringing specialized knowledge of global disclosure requirements and standards to study teams, providing guidance on best practices.
• Oversee interns, contractors, or training of more junior CTDT team members.
• Serve as super-user for the disclosure and transparency tracking, logging and authoring tool.
• Support the assessment and implementation of AI projects for registration and results posting work.
• Contribute or have ownership of the development of training manuals, working instructions or standard operating procedures (SOPs).
• Support or lead process improvement initiatives for CTDT as required.
• Represent CTDT on project teams and/or CTDT collaborative initiatives.

Qualifications

• Bachelor's degree in Life Science with relevant writing expertise or in English/Communications with relevant science expertise. Advanced degree and/or professional certification/credentials preferred.
• 6+ years of experience in Clinical Trial Disclosure and Transparency in the sponsor and/or CRO setting.
• Expert understanding of global regulatory requirements for clinical trial disclosure.
• Superior working knowledge and familiarity with ClinicalTrials.gov and EudraCT/EU CTIS
• Detail-oriented with excellent inter-personal and communication skills
• Strong ability to work both independently and with a team in a global cross-cultural environment.
• Successful track record of managing multiple projects in a fast-paced and deadline-driven environment.
• Excellent communication skills and ability to deliver clear messages to varied audiences.
• In-depth knowledge of Good Clinical Practices, FDA regulations, ICH guidelines, and the drug development process.
• Impeccable attention to detail and ability to complete writing assignments in a timely manner.
• Must be proficient with Microsoft Windows, Word, Excel, Power Point, and other Office applications.
• Experience with AI such as CoPilot and other AI applications.

About Alnylam

We are the leader in RNAi therapeutics - a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.

At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.

Before applying, please review Alnylam's Candidate Privacy Notice regarding how Alnylam handles Personal Data you provide with your application for employment.

The pay range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incen