Program Manager, Oncology

Full Time in Natick, MA

Reporting to the Chief Scientific Officer, the candidate will be an experienced, self-motivated and resourceful Program Manager joining a team and coordinating efforts leading to pre-clinical and clinical development to help execute our vision.  


Job Responsibilities

  • Work with management to plan and oversee project coordination between internal research and third party CRO teams to ensure flawless project execution, on time and within budget, keeping stakeholders informed throughout

  • Assist in the definition of project objectives and scope, involving all relevant stakeholders and ensuring technical feasibility

  • Develop detailed project plans to monitor and track progress

  • Take the lead in monitoring, communicating and controlling project flow to ensure timely coordination of all project team efforts

  • Work with senior leadership to manage changes to project scope, project schedule and costs

  • Consider project risks, report and escalate to management as needed

  • Manage relationships with expert CRO vendors and all stakeholders

  • Track project performance to analyze successful completion of short and long-term corporate goals

  • Create and present project updates to management, enabling participation in overall resource planning


Requirements

  • BS or MS in life sciences with a minimum of 6+/ 4+ years of pharmaceutical industry experience respectively required

  • Proven work experience in program management in early-stage life science, small molecule development experience preferred  

  • Ability to multitask, independently organize time and plan specifics of interdisciplinary work

  • Experience with generating timeline driven development project planning scenarios

  • Excellent communication and interpersonal skills demonstrated in a team environment

  • Excellent partner/vendor-facing and internal written and verbal communication skills

  • Organizational skills and judgement: attention to detail, problem solving ability, and skills in coordinating inputs from diverse stakeholders in a multi-disciplinary environment

  • Accountability: Responsible for executing R&D plans as agreed to with the project team, with responsibility for the quality and timeliness of drug discovery planning that result in reports required for internal decision-making


PLEASE PROVIDE A RESUME AND COVER LETTER BY CLICKING THE "Apply Now" BUTTON BELOW OR EMAIL TO CAREERS@PICTHERAPEUTICS.COM.   THANK YOU FOR YOUR INTEREST.

 

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