Sr. Manager / Associate Director, Program Management at Merida Biosciences

Cambridge, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Aug, 26

Salary

160000.0

Posted On

05 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Program Management, Project Planning, Budget Management, Resource Forecasting, Cross-functional Leadership, Risk Mitigation, Regulatory Filings, Drug Development, Clinical Operations, Regulatory Affairs, Manufacturing, Quality Assurance, OnePager, Smartsheet, ThinkCell, Stakeholder Management

Industry

Biotechnology Research

Description

Description Sr. Manager / Associate Director, Program Management At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively and eliminate the root causes of autoimmune and allergic diseases, and to achieve deep, durable responses while preserving essential immunity. We are looking for passionate individuals to join our mission to transform treatment paradigms across the spectrum of antibody-driven diseases. We are seeking a Program Manager (Senior Manager / Associate Director) to lead a cross-functional program team and drive the successful execution of one of our post DC programs from early-stage research through the initial regulatory filing and into the clinic. This role is critical in ensuring that project goals are achieved on time, within scope, and budget, while maintaining compliance with regulatory standards and fostering collaboration across internal and external stakeholders. The qualified individual will report to the Senior Director of Program and Portfolio Management and will be a partner in building out various initiatives and processes that will be established as the broader organization grows. Key Responsibilities Support the Program Lead in facilitating and executing the Asset Development Team to progress the molecule towards the clinic Develop and maintain detailed project plans, timelines, budgets, and resource forecasts to serve as the one source of truth for the program Function as Program Manager for the research portfolio Coordinate cross-functional teams within R&D, including non-clinical, clinical operations, regulatory affairs, manufacturing, and quality assurance Drive and monitor project progress, identify risks, and implement mitigation strategies Serve as the primary point of contact for key functional leads Lead project team meetings, drive decision-making, and foster a collaborative environment Manage project budgets and support financial forecasting and reporting Other duties assigned, including assistance with other organizational support activities such as resource forecasting and portfolio timeline maintenance Requirements Qualifications: Bachelor’s degree in Life Sciences, Biotechnology, Pharmaceutical Sciences, or related field 5+ years of project management experience in the biotech, pharmaceutical, or life sciences industry Proven track record in leading complex, multi-disciplinary projects through various stages of development, to include regulatory filings Knowledge drug development processes and regulatory pathways Strong communication, leadership, and organizational skills. Proficiency with project management tools (e.g.,OnePager, Smartsheet, ThinkCell, etc) Preferred: Advanced degree (MS, MBA, or PhD) in a scientific discipline Both Research and early Development PM experience PMP or equivalent project management certification Experience working in a fast-paced, startup biotech environment Compensation: We understand that compensation is an important part of considering a new opportunity. Our goal is to be transparent so there are no surprises at the end of the process, and you can feel confident that your offer is both fair and equitable. To support that, we’re sharing our hiring range for this role upfront: typically for the Senior Manager level we target $130,000 to $160,000 The final offer will take into account a number of factors, including your skills, experience, location, market data, and internal equity. Along with a competitive salary, we’re proud to offer a comprehensive benefits package designed to support you both personally and professionally. Merida Biosciences is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited

Responsibilities

Lead cross-functional program teams to drive the execution of post DC programs from early research through regulatory filing and clinical entry. Manage detailed project plans, budgets, and resource forecasts while coordinating between R&D, clinical operations, and regulatory affairs.