Career Opportunities with Seres Therapeutics, Inc.

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Careers At Seres Therapeutics, Inc.

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Clinical Research Liason - Southern Region (USA)

Department: Medical
Location: Cambridge, MA

Why Seres Therapeutics

At Seres Therapeutics, we have a singular mission to transform the lives of patients by targeting the underlying cause of their diseases.  We are pioneers and explorers, charting a new course.  You’ll have the opportunity to truly define your area of focus.

If you have a pioneering spirit, join us as we ignite a revolution in the treatment of disease through the microbiome.

What’s Your Mission?

You 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.

What You’ll Do

  • Develop and maintain rapport with clinical investigators, clinical research organizations (CRO) and research institutions to initiate and expedite clinical studies on investigational new drugs
  • Develop and maintain relationships with study-center healthcare providers, including clinical trial investigators, study nurses/coordinators, data coordinators, and other study professionals to support patient recruitment activities
  • 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
  • Work with CRO personnel (CRAs, CTMs, PM’s) to ensure proper study conduct, review trends and help develop mitigations for implementation
  • Monitor progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements.

What You’ll Bring

  • At least 5 years of previous experience as, monitoring/clinical research associate, clinical study coordinator or clinical project management experience of industry sponsored clinical trials
  • Applied understanding of any applicable regulations (e.g., Good Clinical Practices, ICH guidelines, FDA CFR, ISO, clinical research ethics, HIPAA and patient privacy laws, EU Directive, etc.)
  • 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
  • Ability to handle and prioritize multiple therapeutic areas and projects simultaneously
  • Experience working independently in a regional area with remote or minimal supervision
  • The successful candidate should have the ability to travel up to 50% to domestic locations

You May Also Bring

  • Prior experience guiding and mentoring clinical study staff, and patient recruitment and strategic patient recruitment planning experience is highly desirable
  • Competencies and essential skills in the following: cross functional relationships, decision making, execution/results/process improvement, customer satisfaction
  • Experience with Regulatory and Quality Assurance audits

Who We Are

Seres Therapeutics is a clinical stage biotherapeutic company focused on discovering and developing Ecobiotic™ therapeutic products, novel drugs to treat important diseases by targeting the underlying biology of the human microbiome.  Founded by Flagship VentureLabs, Seres is pioneering the first therapeutics that catalyze a shift to health by augmenting the biology of the microbiome.  Current candidates span infectious, metabolic, and inflammatory diseases.  For more information, please visit

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