MOMA Therapeutics is looking for a Director, Program Management

Imagine joining a company where you…

• Will be part of an experienced and resilient team that is collectively unstoppable, trusts one another, and selflessly collaborates
• Will be part of a group comprised of incredible humans who are committed to the discovery of transformative medicines for cancer patients
• Are needed… because patients are counting on you

About MOMA Therapeutics

At MOMA Therapeutics, we are motivated by a single common goal, to discover and develop innovative new medicines for patients through our singular focus: the therapeutic targeting of molecular machines.

In this role you will… 

Play an instrumental role in organizing and advancing critical portfolio programs, facilitating timely and impactful decisions, and contributing to the development of overall program strategy at MOMA Therapeutics. Together with program leaders, this individual develops integrated drug discovery and development plans for the selection and progression of oncology clinical candidates into clinical development and registration. In this role you would also ensures organizational alignment and oversee program execution at MOMA and CROs.

Job Responsibilities:

• Leads program management activities for one or more small molecule cancer therapeutics through development candidate selection to clinical Proof of Concept (POC) and into full development and registration.
• Supports the discovery program team in the development of the program strategy for selection of the development candidate and progression into clinical development by planning and tracking activities in pharmacology, toxicology and ADME studies, preclinical, and indication expansion, drug supply and formulation development and clinical planning and operations.
• Supports the development team through clinical development by creating and executing on an integrated clinical plan for POC and registration. Works with sub-teams in clinical operations, safety, regulatory to ensure that functional activities are fully integrated into the clinical development plan and support indication expansion and regulatory approval.
• Achieves organizational alignment and seamless execution of the integrated drug discovery and development plans by working cross-functionally within MOMA and with CROs.
• Tracks program progress against the plan, working with department heads to identify and resolve resource constraints consistent with corporate priorities.
• Schedules, facilitates, documents, and ensures uniformity between programs including agendas, meeting minutes and other program documentation.
• Supports CMO/CDMO selection, oversight, and relationships

About you…

• You have 7 years overall experience in drug development with at least 5 years of program management experience in the biopharmaceutical industry, with small molecule Oncology experience preferred
• You have an advanced Degree (MBA, MS, PharmD, PhD)
• Established contacts and relationship building experience with external vendors including CMOs and CDMOs
• Experience in at least one of the functions related to pharmaceutical development (e.g. Research, Regulatory Affairs, Clinical Dev/Operations, CMC) is required
• You have demonstrated trust, transparency, and clear communication
• You are a highly collaborative team player who fosters open communication and facilitates mutual understanding and cooperation between all stakeholders
• You have strong interpersonal skills with the ability to motivate others, influence without authority, and negotiate conflict situations
• You are able to work in a highly complex, multi-cultural, often stressful environment
• You are highly effective communications skills – written and verbal
• You are able to manage multiple tasks of varied complexity simultaneously with excellent organizational skills
• You are proficient in Microsoft Office Suite, SharePoint, and working knowledge of project management software such as Microsoft Project, Office Timeline, One Pager, etc.
• You work hard, you are kind to others, and you enjoy being a part of a kick-ass collaborative team that gets stuff done
• You enjoy being in an environment where scientific data rules the day