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Senior Manager, Clinical Project Management

Remote

 

About Apogee Therapeutics
Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally.
Apogee Therapeutics, Inc. is a biotechnology company seeking to develop differentiated biologics for the treatment of atopic dermatitis, chronic obstructive pulmonary disease and other inflammatory and immunology indications with high unmet need. Our antibody programs are designed to potentially overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. We seek to reshape the current standard of care for inflammatory and immune diseases because we believe people living with these diseases deserve the best possible treatment, and we refuse to stop at “good enough.”
We are a fast-paced company committed to building an exceptional company culture, founded on our C.O.R.E. values: Caring, Original, Resilient and Egoless. 
If this sounds like you, keep reading!

 

Role Summary

We are seeking a highly skilled Senior Clinical Project Manager to join our dynamic clinical team. You will provide project management support to cross-functional teams advancing Apogee’s development programs.

Reporting to the Clinical Chief of Staff, this position requires a self-starter who can organize projects effectively in a rapidly growing, fast-paced setting. If you are a skilled PM, eager to contribute to quickly progressing clinical programs, and thrive in a culture of growth and camaraderie, this role is for you. The ideal candidate will have project management experience in clinical drug development, excellent organizational skills, and a proven track record of successfully managing complex projects.

Key Responsibilities 

  • Support planning, tracking, and execution of clinical programs from pre-IND through clinical stages.
  • Develop detailed project plans and timelines, dashboards, trackers, and other project management or productivity tools using Smartsheet/ Office Timeline Pro+/ think-cell.
  • Create and maintain project documentation including agendas, minutes, project timelines, and decision logs as relevant.
  • Coordinate cross-functional, clinically-focused teams to update and maintain integrated program timelines.
  • Plan and facilitate meetings of cross-functional teams to discuss key questions and open workstreams needed to advance our clinical programs.
  • Foster and support active communication and information flow between team members and relevant stakeholders to ensure projects adhere to objectives, milestones, and deliverables.
  • Proactively identify potential risks and challenges that could impact project timelines, quality, or budget. Help to identify potential risk mitigation strategies.

Ideal Candidate 

  • Bachelor’s or higher degree in science or equivalent related discipline.
  • 3+ years of experience in the biopharmaceutical industry.
  • Project management experience required; PMP certification is a plus.
  • Experience with regulatory submissions (IND, NDA) is a plus.
  • Proven ability to plan and manage complex projects and coordinate cross-functional teams.
  • Excellent organizational and problem-solving skills.
  • Strong interpersonal and communication skills, with the ability to collaborate effectively with diverse stakeholders and communicate effectively at all levels of the organization.
  • Experience with project management tools and best practices with a demonstrated ability to tailor to the specific needs of the team, management, and company culture.
  • Proficiency in Smartsheet and/or MS Project, ability to create and update Gantt charts and generate reports, experience with MS Teams, Office Timeline Pro+, think-cell.
  • Astute attention to detail.
  • Comfort asking detailed questions and raising potential concerns to ensure clarity of understanding and tight cross-functional coordination.
  • Ability to manage multiple ongoing projects within a fast-moving organization.
  • Demonstrated ability to synthesize details into takeaways and implications that can be shared with a wide audience.
  • Proactive and adaptable, with a strong commitment to continuous improvement.
  • Ability to travel up to ~20% per year including quarterly All Hands meetings and team meetings.

The anticipated salary range for candidates for this role will be $125,000-$150,000/year. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. 

 

What We Offer
  • A great culture, grounded in our C.O.R.E. values: Caring, Original, Resilient and Egoless
  • Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly
  • Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
  • Flexible PTO
  • Two, one-week company-wide shutdowns each year
  • Commitment to growing you professionally and providing access to resources to further your development
  • Apogee offers regular all team, in-person meetings to build relationships and problem solve
 
E-Verify Participation: As part of the I9 verification of authorization to work in the US, Apogee participates in E-Verify. To learn more about E-Verify please review this poster.
 
Apogee Therapeutics is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
 
To review our privacy policy, click here

 

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