Principal Scientist, Bioanalytical Sciences (Outsourcing Vendor Management)

The Bioanalytical Sciences group at Alnylam is seeking a highly motivated candidate to join our team to help advance novel RNAi therapeutic programs from discovery to the clinic.
This individual will be responsible for managing outsourced efforts to design and implement fit-for-purpose methods across various platform technologies, as well as the subsequent use of these assays for nonclinical or clinical bioanalytical sample analysis to inform on target engagement, downstream pharmacodynamics (PD), pharmacokinetics (PK), mechanism of action, safety, and immunogenicity to advance RNAi therapeutic development.
The ideal candidate will have expertise in bioanalytical platform technologies and experience in regulated (GLP, GCLP) bioanalysis, with exceptional communication and interpersonal skills to effectively collaborate with multiple project teams and provide bioanalytical support. This is an exciting opportunity to join a vibrant team and interact with highly motivated scientists across a broad array of disciplinary expertise areas.

This position is onsite and will be primarily located in Cambridge, MA.

Key Responsibilities

* Provide scientific support for CRO efforts in the design, development, and implementation of a variety of analytical methods in a regulated (GLP, GCLP) environment.
* Serve as a subject matter expert in the application of bioanalytical techniques (LC-MS, ELISA, MSD, PCR, cell-based assays) to support PK, PD, biomarker, or immunogenicity objectives in nonclinical or clinical studies.
* Leverage depth of knowledge and hands-on experience with bioanalytical techniques to advise on assay design, method validation design, and interpretation of method performance data.
* Collaborate with Alnylam bioanalytical scientists to ensure successful method transfer and continuity in PK or PD biomarker testing from discovery through development.
* Participate in program team meetings, serving as a collaborative and reliable bioanalytical representative and team member to meet study timelines and drive programs forward.
* Participate in regular vendor meetings, provide critical reagents, review study plans, data transfer agreements, data and reports.
* Ensure delivery of quality bioanalysis data and reports according to timelines.
* Apply creative problem-solving skills to address any issues that arise during assay development or sample analysis.
* Review bioanalytical contracts to ensure the scope of work accurately reflects project goals.
* Participate in writing and reviewing regulatory documents for initiation of clinical studies (such as IND and CTA) and drug approvals (such as NDA and MAA).

Qualifications

* PhD in biochemistry, chemistry, molecular/cell biology, or related field with 6+ years of relevant industry experience, or non-PhD with 10+ years of experience.
* Hands-on experience with the use of bioanalytical techniques such as ELISA, MSD, LC-MS, PCR, or cell-based methods to support PK, PD, or immunogenicity evaluations.
* Has previous experience in conducting or managing regulated (GLP, GCLP, CLIA) bioanalysis studies.
* Has experience in overseeing CRO bioanalysis work and/or direct experience as CRO scientist/principal investigator with sponsor interactions.
* Experience with writing or reviewing bioanalytical reports and contributing to regulatory submissions.
* Demonstrates a solid understanding of disease biology and the drug development process to enable design and implementation of assays that are fit for intended use.
* Strong relationship-building skills in working in a matrixed environment with both internal and external stakeholders.
* Possesses the ability to think creatively and strategically with strong problem-solving skills.
* Experienced with the drug approval process and the bioanalytical clinical development of nucleic acid (siRNA, ASO, mRNA, gene therapy), biologic, or small molecule drugs.
* Organized and detail-oriented with the ability to multi-task and handle multiple projects.
* Has excellent interpersonal and communication skills to enable effective collaboration with cross-functional teams.

About Alnylam:Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality.

Our culture:Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others.

At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients.