Project Manager, Clinical Development – TEMP

Title: Project Manager, Clinical Development

Location: California – Remote

Type: Contract

Rate: 85-100/hr depending on experience

Start Date: ASAP

Leading Pharmaceutical Company located in CA is hiring a Project Manager, Clinical Development w/5 years industry experience. If you want to be a part of this groundbreaking work, please apply!

SUMMARY/JOB PURPOSE:

The Project Management Director partners with cross-functional project teams to develop and maintain project plans, Gantts/timelines, status reports, strategic development and filing plans. Oversees and manages the operational aspects of ongoing oncology drug development projects (IND-enabling, Phase 1 to 3, NDA/BLA filing submissions) and serves as liaison between project teams and executive management.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Responsible for directly managing several clinical development projects and providing direction, management, and assistance to the Development Team Leader (DTL), Clinical Development Lead (CDL) and/or Franchise Team Leader (FTL) and project teams.

Works in partnership with the DTL/FTL and project team to develop and gain approval of the project strategy.

Drives project execution through the development and implementation of high quality, integrated cross-functional project plans.

Identifies risks and issues which pose a challenge to achieving strategic goals; develops and implements plans to mitigate risks, resolve issues and execute corrective actions.

Co-chairs team meetings, prepares high quality meeting minutes and ensures that program information is communicated to team members and other project customers. Coordinates communication within the organization as well as with external business partners, consultants or CROs.

Facilitates team discussion and agreement on clear, concise program goals. Measures and reports progress against agreed milestones. Develops options and recommendations for moving plans forward to maintain milestones and goals.

Education/Experience:

BS/BA degree in related discipline and 13 years of related experience; or,

MS/MA degree in related discipline and 11 years of related experience; or,

PhD in related discipline and 8 years of related experience; or,

Equivalent combination of education and experience.

PMP or equivalent certification is preferred.

Experience/The Ideal for Successful Entry into Job:

At least 5 years of experience managing cross-functional development-stage projects in the biotech/pharmaceutical industry.

Experience managing oncology projects and/or development of biologics is preferred.

System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.