What are the responsibilities and job description for the Sr. Manager / Associate Director, Program Management position at Merida Biosciences?
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
Qualifications:
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
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
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)
- 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
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
Salary : $130,000 - $160,000