Career Opportunities with Seres Therapeutics, Inc.

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Careers At Seres Therapeutics, Inc.

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Clinical Research Liaison - Mid West USA

Department: Clinical Operations
Location: Cambridge, MA

Clinical Research Liaison

What’s in it for you? 

Seres Therapeutics is well-positioned to become the first company to bring an approved microbiome drug to patients through our proprietary discovery and design platform. We identify key alterations in the microbiome that are associated with specific diseases, and are designing live bacterial ecologies to act as therapeutics. We are currently conducting multiple clinical trials including a recently started Phase III study.  Seres is a dynamic and well-financed biotechnology company headquartered in Cambridge, MA.

The Clinical Research Liaison (CRL) will serve as a key liaison between Seres Clinical Operations group and the sites and site personnel (e.g. study coordinators, investigators) for Seres clinical trials to ensure optimal conduct and implementation of Seres trials with regards to enrollment and compliance with GCP and regulatory requirements. The CRL will develop and maintain professional relationships with study-center healthcare providers, including clinical trial investigators, study nurses/coordinators, data coordinators, and other study professionals to support patient recruitment activities. In addition, the CRL will be a resource for study monitoring or clinical study management to Seres Clinical Operations.

You will serve as key liaison between Seres Clinical Operations group and the sites and site personnel (e.g. study coordinators, investigators), engage and establish relationships with clinical site personnel conducting Seres clinical trials through on-site meetings and interactions to continuously support patient recruitment activities, and serve as a clinical trial resource for sites and site personnel. This position will work closely with sites and site personnel to develop study and/or site patient recruitment and retention tactics and strategies appropriate to the individual study needs, and generate and monitor enrollment modeling scenarios and continuously evaluate the recruitment projections for improvements or triggers to support the implementation of action and/or contingency planning. Additionally, you will coordinate with clinical study staff to identify and interact efficiently to maximize use of site resources for effective study recruitment, provide effective presentations to sites, site personnel, groups, and participating in 1:1 discussions, tailoring discussions to meet specific recruitment needs, and serve as a study-specific educational resource to the Seres clinical trial study site personnel. You should also be keen to maintain a high standard of integrity and professionalism in the Seres study-site community, keep abreast of changes in treatment trends that could impact Seres clinical trials, and maintain operational, GCP and regulatory compliance at all times.

How do you know if you’re the right fit?

You should have a minimum of a BA/BS degree in a life science field or other relevant discipline if paired with commensurate clinical trial experience and at least 2 years previous experience as clinical study coordinator, monitoring/clinical research associate or clinical project management experience of industry sponsored clinical trials; knowledge of drug development process and FDA and ICH regulations and guidelines. Additional experience should include demonstrated computer skills (MS Office, MS Project, PowerPoint), strong business communication skills (written; verbal; presentation), and initiative and ability to identify issues and create solutions. Prior experience guiding and mentoring clinical study staff, and patient recruitment and strategic patient recruitment planning experience is highly desirable. The successful candidate should have the ability to travel up to70% to domestic locations.



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