Senior Project Manager - Clinical

Location
San Diego, CA
Posted
Aug 28, 2018
Required Education
Bachelors Degree
Position Type
Full time

Tocagen is a clinical-stage, cancer-selective gene therapy company focused on developing first-in-class, broadly applicable product candidates designed to activate a patient’s immune system against their own cancer from within.

Every member of our team plays a significant role in our success. Tocagen hires individuals who share our passion for ending cancer mortality and have exceptional talent that will contribute to this goal.

Function/Scope:

The Project Manager will be responsible for ensuring the scope and direction of programs through all stages of the candidate development process, including Phase 1-3 clinical development studies. This position will be able to develop and manage detailed project plans, drive the matrix project teams to achievement of key milestones, and facilitate communication throughout all levels of the organization. In addition, the Project Manager may play a leadership role in the future development of new programs such as investigator-sponsored trials (IST), compassionate use and named patient protocols.

Duties and Responsibilities Include But Are Not Limited To:

  • Applies Project Management best practices in the development, initiation, planning, execution, control and closing of projects
  • Develops detailed project plans and timelines and tracking of key deliverables and milestones for preclinical and clinical programs
  • Manages day to day project activities for the Program Teams
  • Responsibility for project performance, risk management, and issue resolution at the project team operations level
  • Represents, in partnership with the Program Lead, the teams and programs at Sr. Management meetings and participating in and/or leading project reviews
  • Facilitates communication and has demonstrated ability to share complex information with diverse audiences across all levels within the organization
  • Provides support for new pipeline assets transitioning from research to the clinic
  • Performs other duties as required

    Qualifications:

  • A strong track record of leading teams to evaluate new therapies in the pharmaceutical industry (oncology or gene therapy experience preferred).
  • Technical experience in a discipline associated with drug development is required
  • Knowledge of issues that drive early and late stage development projects and proven ability to develop and manage complex project plans, timelines and critical path tasks is required
  • Excellent written and verbal communication as well as interpersonal, negotiation and conflict resolution skills are essential
  • Strong organizational, analytical, and time management skills with demonstrated ability to effectively multitask and advance various projects simultaneously
  • Ability to hold oneself and others accountable for commitments in a productive and assertive manner
  • Ability to drive consensus and decision making
  • Innovative and collaborative spirit
  • Must be able to prioritize and work effectively in a constantly changing environment.
  • General understanding of the FDA, EMA, ICH and other guidelines relevant to the pharmaceutical industry
  • Previous experience with preparation of a NDA/BLA is desirable

Education and Experience:

  • An Advanced Degree (PhD, MS) or equivalent experience in a relevant scientific and/or Project Management discipline is required; PMP certification is highly desirable.
  • Five to 7 years in biotech/pharma industry along with relevant project management experience managing drug development programs
  • Experience with biological products or cancer immunotherapeutics is desirable, but not required
  • Proficiency in Microsoft Office suite applications and high-level of proficiency in Microsoft Project