Senior Clinical Data Manager - Cambridge - Alnylam

Description

Senior Clinical Data Manager

The Sr. CDM will lead and contribute to data management activities in support of Alnylam studies across all stages of clinical drug development.

This position reports to the Director, Clinical Data Management.

Summary of Key Responsibilities

• Contribute to data management activities as a lead study data manager in support of Alnylam clinical studies
• Lead database build activities including leading cross-functional review of eCRF content, review of edit check specifications, and perform user acceptance testing
• Monitor data collection, coding, and cleaning by vendors through tracking of study metrics and targeted data reviews
• Oversight of database lock activities and ultimate archiving of study data
• Collaborate with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Global Patient Safety and Risk Management, and Regulatory Affairs; CROs, central and local laboratories, and other vendors
• Establish cross-functional, internal data review plans, coordinate data cuts/transfers, and conduct data reviews
• Review CRO data management plans, CRF completion guidelines, external data transfer specifications and other study documentation
• Contribute to development and implementation of department workflows and infrastructure strategy (such as preferred provider interactions, SOPs, and templates) that reflects data collection standards, consistent with industry best practice and regulation
• Represent data management and effectively communicate requirements, strategy, timelines and deliverables at internal cross-functional team meetings and meetings with external vendors
• Participate in the training of external vendors and site staff
• Participate in the drafting and/or review of timelines consistent with company goals and ensure all deliverables and milestones are met
• Review clinical protocols/amendments, clinical study reports, statistical analysis plans, etc.
• Support GCP inspection readiness
• Demonstrate clear alignment with Alnylam Core Values including, Commitment to People, Innovation and Discovery, Sense of Urgency, Open Culture and Passion for Excellence

Qualifications

• BS/BA in scientific discipline,
• At least 7 years related experience in a pharmaceutical/biologics/biotechnology company
• Experience working in clinical drug development through Phase 3 in an outsourced CRO model; experience with drug development in rare genetic diseases preferred
• Expert knowledge of eClinical processes, efficient design/build of an EDC data management system and other Clinical Trial/Data Management Systems
• Knowledge and understanding of regulations and industry/adopted data standards such as CDISC, SDTM, and CDASH
• Experience working with Oracle InForm and Medidata Rave
• Experience using standardized medical terminology, including MedDRA and WHODrug
• Experience working with MSOffice Suite (Excel, Word, PowerPoint) and familiarity with MS Project
• Excellent written and oral communications skills
• Highly motivated and flexible, with excellent organizational and time management skills
• Ability to work independently and as part of a multi-disciplinary team
• Understanding ofICH GCP as well as general knowledge of industry practices and standards
• Knowledge and understanding of regulatory requirements and expectations for clinical data systems including 21 CFR Part 11
• NDA/MAA experience

Alnylam Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment.

U.S. Pay Range

$131, $178,300.00

The pay range 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 incentive) and an annual long-term incentive award (e.g., equity).

Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.

Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website:

AboutAlnylam

We are the leader in RNAi therapeutics- a revolutionaryapproach 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 possibleand 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, wherean authentic, inclusive culture and breakthrough thinkingfuel 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.

>