Job DescriptionProject Manager
Are you ready to uplevel your career? Join an innovative biopharmaceutical company and be part of our exciting journey!
We are looking for a Project Manager to join our team.
Working with Us
At Y-mAbs Therapeutics (NASDAQ: YMAB), our mission is to become the world leader in developing better and safer radioimmunotherapy and antibody-based oncology products addressing clear unmet pediatric and adult medical needs. With the right partnerships and collaborations, we envision changing the course of cancer treatment and improving outcomes for patients and their families.
We have offices in
Princeton, New Jersey (US) and
Hørsholm, Denmark (near Copenhagen). We also have a laboratory based in
Nutley, New Jersey (US).
Y-mAbs has an exciting future ahead. If you are passionate about being part of a truly patient-centric organization focused on developing and commercializing cutting-edge therapies to treat a variety of cancers, we want to hear from you!
About the Role
The Project Manager will support day-to-day execution of projects within Y-mAbs, ensuring completion on time, within scope, and budget across the entire company. This role offers a great opportunity to collaborate across various functions in a biotech company and gain comprehensive insight into the drug development process.
Key Responsibilities
- Support teams in the development of detailed project plans, including timelines, milestones, and resource allocation.
- Lead and manage multiple projects from initiation to completion, ensuring they are delivered on time, within scope, and within budget.
- Coordinate and communicate with cross-functional teams, stakeholders, and clients to ensure project alignment and success.
- Identify and communicate project risks and issues, to the relevant stakeholders and head of project management office
- Monitor project progress and prepare regular status reports.
- Facilitate project meetings, including kick-offs, status updates, and post-project debriefs.
- Ensure compliance with company policies, procedures, and quality standards.
- Foster a collaborative and positive team environment.
Key Qualifications
- In-depth knowledge of drug development processes, regulatory requirements, and industry best practices.
- Bachelor's or Master’s degree in Life Sciences, Biotechnology, or related field (Ph.D. preferred).
- At least 2 years of experience in project management in biotechnology or pharmaceutical company or at least 4 years of experience in consulting at a project management capacity.
- Extensive experience in managing complex projects within the biotech/pharmaceutical industry, working cross-functionally with research and development, regulatory affairs, clinical, medical and other departments to achieve company objectives.
- Strong leadership, communication, and interpersonal skills, with the ability to influence and collaborate with senior stakeholders.
- Exceptional organizational and multitasking abilities.
- Expertise in project management software and tools (e.g., MS Project)
