Celgene Senior Manager, Project Management - Pharmaceutical Development and Ops in Summit, New Jersey
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.
Senior Project Manager, Global Pharmaceutical Development and OperationsSummit, NJ
Executive Director, PMO, Business Strategy and Integration
Business Strategy and Integration, Global Pharmaceutical Development and Operations
Bachelor’s degree with a minimum of 7 years of experience – at least 5 yrs in Pharma and 3 yrs in Project Management or equivalent preferred. PMP certification desirable.
This global position will support one or more CMC Development and/or Technical Commercialization Teams within Global Pharmaceutical Development and Operations (GPDO). He/she will be responsible for the management of the day-to-day activities for these programs. He/she is accountable to the BioCMC Team Leads, Compound Leaders and Technical Commercialization Leaders to manage critical path activities and risks, as well as to assist in the development of contingency plans, and to manage overall project planning, cross-functional team meetings, and the development of updates and presentations for management. This role requires the ability to develop and maintain strong collaborative and cooperative working relationships with team members across different functions and at different levels within the organization.
The roles and responsibilities include, but are not limited to, the following:
Manage multiple, low to medium complexity cross-functional CMC Development and/or Technical Commercialization projects, with a focus on helping to develop the program strategy with the team leader, as well as driving the execution of the program
Effectively manage team meetings, including the scheduling of meetings, the preparation of agendas, the development of meeting minutes, and the follow up on action items, while doing so using the standardized tools developed within the department.
With input from the Leader and the team members, lead the team in the development of an integrated timeline, while ensuring that GPDO team timelines are aligned with the Global Project Team timelines
Tracks the various parts of the timeline with the sub-teams and brings issues to the leader’s attention
Serves as a member of sub-teams to assure that functional deliverables are completed on time, on budget, and according to quality standards
Proactively identify program risks and work with the team and team leader to develop contingency plans
In conjunction with the team and team leader, develop critical path analyses to identify potential ways to accelerate timelines, reduce costs or mitigate risks
Working with the team and team leader, contribute to the development of annual team goals and objectives, as well as team presentations for Governance Committee meetings
Responsible for the preparation of monthly status reports, including those for the GPDO Leadership Team
Promote a culture of collaboration, cooperation, execution excellence, effective communication and cross-functional problem-solving to become a high-performing team.
Ensure that team recommendations related to project direction, timelines and budget which need endorsement by Steering Committees are planned for review by the Committees at the appropriate timepoints
Experience with Biologics development.
Broad knowledge of the drug development process
Strong analytical, problem-solving, and critical thinking skills
Demonstrated ability to earn the trust of team members and management
Must be able to interact and communicate effectively at all levels of the organization
Must be competent in Project Management tools and methodologies
Excellent organizational and time management skills
- Bachelor’s degree with a minimum of 7 years of experience – at least 5 yrs in Pharma and 3 yrs in Project Management or equivalent preferred. PMP certification desirable.
Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.COMMITTED TO IMPROVING THE LIVES OF PATIENTS WORLDWIDE
At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients. Our vision as a company is to build a major global biopharmaceutical corporation while focusing on the discovery, the development, and the commercialization of products for the treatment of cancer and other severe, immune, inflammatory conditions.
“At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients.”
There are more than 300 clinical trials at major medical centers using compounds from Celgene. Investigational compounds are being studied for patients with incurable hematological and solid tumor cancers, including multiple myeloma, myelodysplastic syndromes, chronic lymphocytic leukemia (CLL), non-Hodgkin’s lymphoma (NHL), triple-negative breast cancer and pancreatic cancer. As committed as we are to clinical accomplishment, we are equally committed to patient support, which is a guiding principle at Celgene. We believe all who can benefit from our discoveries should have the opportunity to do so. Celgene puts patients first with industry-leading programs that provide information, support and access to our innovative therapies.