About this opportunity
Hengrui USA lists this Clinical PPM Senior Manager / Associate Director opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Clinical PPM Senior Manager / Associate Director
(Bilingual: English & Mandarin | Oncology & Non-Oncology)
Department: Clinical Development
Reports to: Chief of Staff to the CMO office
Location: Boston, MA (hybrid; minimum 3 days/week in office)
Position Overview
We are seeking a Clinical Program Senior Manager / Associate Director to support our growing clinical development portfolio. This role will work closely with the Chief of Staff to the CMO and cross-functional program teams to coordinate and drive the execution of ongoing clinical development activities across oncology and non-oncology programs. A key focus of the role is to bridge, streamline, and coordinate ex-local and local clinical development programs, ensuring alignment of plans, timelines, and decisions across regions.
Key Responsibilities
Bridge, streamline, and coordinate ex-CN and China clinical development programs to ensure alignment across regions and teams.
Track program timelines, milestones, and deliverables across multiple studies and development initiatives.
Facilitate cross-functional collaboration across Clinical Development, Clinical Operations, Regulatory Affairs, Biometrics, and Translational teams.
Organize and support cross-functional program meetings and development reviews, including agenda preparation, meeting minutes, and action item tracking.
Maintain integrated development timelines and ensure alignment across internal teams.
Identify program risks and proactively coordinate mitigation strategies.
Support preparation of development updates, internal reports, and leadership presentations.
Assist in portfolio planning, prioritization, and resource coordination.
Qualifications
4+ years of experience in biotech/pharmaceutical clinical development, program management, clinical operations, or life science consulting (minimum requirement).
Advanced degree in life sciences, medicine, pharmacy, or related field (PhD, MD, PharmD, or MS).
Strong understanding of global clinical development and clinical trial execution.
Experience supporting cross-functional drug development programs.
Highly detail-oriented with excellent organizational skills.
Excellent communication and stakeholder management skills.
Ability to manage multiple programs in a fast-paced environment.
Preferred Experience
PMP certification.
Experience in oncology drug development and/or non-oncology therapeutic areas such as immunology, CVRM or other indications.
Language Requirement
Fluent in both English and Mandarin to support collaboration with global teams and cross-regional stakeholders.
We offer a comprehensive benefits package including medical, dental, and vision insurance; paid time off; a 401k retirement plan with company match. Company paid Life Insurance plan. Additional voluntary benefits (e.g., FSA, DCSA, supplement life insurance, etc.) are available.
Schedule: Monday to Friday
Salary Range:
$165,000–$210,000 annually. Final title and compensation will be determined based on the candidate’s experience, qualifications, and overall fit for the role.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.