Director, Program Management
Watertown, MA
Development – Program Management /
Full-time /
On-site
COMPANY INTRODUCTION
Triveni Bio is breaking new ground in the identification of novel disease targets – working at the convergence of human genetics, best-in-class antibody design, and precision medicine. We are pioneering a Mendelian genetics-informed precision medicine approach to develop functional antibodies for the treatment of immunological and inflammatory (I&I) disorders. Our lead antibody program (TRIV-509) targets kallikreins 5 and 7 (KLK5/7) to directly impact skin barrier function, inflammation, and itch – providing a meaningful and much needed potential treatment option for patients with atopic dermatitis and other barrier disorders. In all the work we do, we adhere to our core values: patient impact, bold and rigorous science, open collaboration, kindness & respect.
SUMMARY
The Director, Clinical Program Management, is a pivotal role within the cross-functional Program Team who leads the planning of workstreams, drives the execution of activities required for successful development, and ensures transparency, alignment, and efficiency across functions. This individual will partner closely Program Leader (PL) and key stakeholders with Clinical Development, Regulatory, CMC, Research, and others to ensure program timelines, budgets, and deliverables are clearly defined, tracked, and achieved. The successful candidate will bring strong organizational skills, scientific acumen, and a proactive mindset to enable seamless communication and effective decision-making. This is a highly visible role with an opportunity to make a significant impact at a dynamic, fast-growing, clinical-stage biotech company.
· Partner with Program Leader(s) to optimize the Program Team’s effectiveness and decision making; facilitate team building and communication, create and drive timelines to keep project(s) on schedule
· Manage the planning and day-to-day execution of projects, ensuring that cross-functional deliverables are achieved, and milestones are met; serve as a central hub for program knowledge, facilitating effective internal communication and stakeholder alignment.
· Develop and maintain integrated program plans; accurately track and provide timely reporting on progress
· Facilitate continuous identification of issues, opportunities, and risks; propose mitigation strategies and drive solutions with Program Team input
· Contribute to development of longer-term strategy for the program in partnership with the Program Leader(s) and R&D management
· Schedule, organize, and drive team meeting(s): prepare and distribute agendas/minutes; identify and track decisions and action items, escalate areas of concern as appropriate
· Collaborate with Program Leaders, Finance, and as appropriate Department Heads to develop and update project budgets; coordinate with Finance and Legal on budget/forecast and document tracking
· Help manage and coordinate program related CRO contracts and work orders
EXPERIENCE & QUALIFICATIONS
· BA/BS in a scientific discipline is required; an advanced degree (PhD, MS, MBA, MD) in a field relevant to drug development is desirable
· 8+ years experience in R&D in pharma or biotech (some experience with small to medium-sized companies is preferred), with a minimum of 5 years in program management on interdisciplinary or cross-functional project teams
· Extensive experience with programs in preclinical/clinical development required; involvement in regulatory submissions, including INDs/CTAs is desirable; some experience with discovery-stage research is desirable
· Broad understanding of biopharmaceutical drug development, including working knowledge of relevant ICH, GLP, and GCP guidance and regulations
· Highly proficient in utilizing project management best practices, project planning, and collaboration tools (e.g., Sharepoint, MS Teams, Smartsheet, etc). Skilled in goal setting, facilitating decision making and prioritization, and time management
· Must have a proactive mindset with strong leadership, facilitation, teamwork, influence management, organizational skills, and ability to work independently
Triveni Bio, along with other biotech companies, has become aware of a surge in email scams targeting prospective job candidates within our industry. Official Triveni Bio applications will always be submitted through Lever, our ATS. Any applications that take you to other platforms could be fraudulent. We do not use text or chat applications to conduct interviews or make job offers. Official Triveni Bio correspondence will always be conducted from email addresses ending in @triveni.bio. Please disregard any other communication that does not originate from this domain name. If you receive any suspicious requests or communications, please verify their authenticity before responding.
