The Role
The Project Manager will oversee pre-clinical programs, manage budgets and timelines, coordinate cross-functional teams, and improve project processes.
Summary Generated by Built In
Company Overview:
We’re looking for teammates who relish challenges and are compelled to leave a positive mark on the lives of the patients we serve. If embracing creativity and candor, thriving on challenges, and empowering your teammates to succeed excites and inspires you, join us as we champion hope and work to advance our aspiration to find therapies for renal disease.
The Role:
We’re seeking a highly motivated and organized project manager with a strong scientific background to oversee the planning, execution, and successful delivery of pre-clinical programs focused on small molecule drug discovery and development. The Project Manager will be responsible for managing timelines, budgets, resources, and risk, ensuring that all program milestones are met on time and in accordance with scientific, regulatory, and quality standards. This is an exciting opportunity to be part of a fast-paced, early-stage biotech company focused on impacting patients in the renal disease space.
Responsibilites
- Lead project team meetings – draft agendas, document key discussion points, actions, and decisions, and maintain program records for easy access by the team.
- Ensure projects are conducted in compliance with industry regulations and organizational quality standards.
- Drive development of program Gantt charts and summarize the critical path in timeline slides for team discussions and leadership meetings.
- Proactively identify risks and potential roadblocks in the project pipeline and develop mitigation and contingency strategies. Communicate plans to senior management and stakeholders.
- Coordinate across various internal functions, including medicinal chemistry and biology teams to drive projects forward, ensure all stakeholders understand their deliverables, and prioritize key workstreams.
- Ensure projects proceed according to agreed timelines and budget, flagging for stakeholders and leadership when a timeline or budget deviation is anticipated.
- Identify resource gaps for projects and highlight the impact to timelines/budget for stakeholders and senior management.
- Perform scenario planning to facilitate team decision making and prepare for multiple potential outcomes.
- Partner with scientific leads and legal team to negotiate and establish contracts with CROs, academic partners, and consultants.
- Provide operational support to program teams, including international and domestic shipping, PO generation, and managing SharePoint folder structure.
- Continuously seek ways to improve our workflows, internal project management processes, and tools.
Qualifications
- Bachelor’s degree in Life Sciences, Pharmaceutical Sciences, Chemistry, or a related field (Master’s degree or PhD preferred).
- PMP certification or equivalent project management training is a plus.
- 2+ years of experience in project management in the biotech, pharmaceutical, or related industry, with a focus on pre-clinical or small molecule drug development.
- Experience working in drug discovery and pre-clinical development stages (e.g., early-stage drug discovery, animal studies, ADME/Tox).
- Strong understanding of small molecule drug development processes, including pharmacokinetics, toxicity studies, formulation, and scale-up.
- Proven ability to manage cross-functional teams, multiple vendors and projects simultaneously.
- Exceptional organizational and time management skills, with an ability to manage competing priorities and deadlines.
- Excellent written and verbal communication skills, with the ability to present complex information in a clear and concise manner.
- Solid problem-solving and critical thinking skills, with the ability to anticipate challenges and address them proactively.
- Proficiency with project management software, such as Smartsheet
- Familiarity with pre-clinical data analysis and reporting tools is a plus.
Education:
Experience:
Skills & Competencies:
We believe in building an inclusive and balanced team. We also know meeting every single-exact-criteria can get in the way of meeting stellar folks. Please don’t hesitate to apply!
Renasant Bio is an equal opportunity employer. We do not discriminate in regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, marital status, ancestry, physical or mental disability, veteran status, or any other legally protected.
Please note that we do not accept unsolicited resumes from recruitment agencies and external recruiters. No fees will be paid for such submissions.
Top Skills
Project Management Software
Smartsheet
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The Company
What We Do
5AM was founded in 2002 and pursues investments in advanced life science innovations, and seeks to be diversified across the biopharmaceutical therapeutics, and platform technologies. Within each sector, 5AM invests across multiple therapeutic areas and modalities and evaluates opportunities based on innovative platform technologies, corporate spin-offs and products with shorter development cycles.
Content 5AM shares on this platform is not, and may not be relied on, in any manner, as legal, tax, investment, accounting or other advice or as an offer to sell or a solicitation of an offer to buy an interest in any private fund, special purpose or other investment vehicle sponsored by 5AM Ventures. Content 5AM shares on this platform is not an investment recommendation.
For a full list of all 5AM portfolio companies, please visit: https://5amventures.com/portfolio/
