Associate Director, Global Program Management
2 weeks ago
**Summary**:
Internal Title: Associate Director #LI-Hybrid Location: Cambridge, MA About the role: This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients Based on our understanding of cancer at the molecular, cellular and organismal levels, Translational Clinical Oncology (TCO) designs and drives innovative early development clinical trials to develop the next generation of highly effective therapeutics that transform the lives of patients with cancer.
**About the Role**:
**Key responsibilities**:
- Provide program management leadership and support at leader level to complex TCO programs, sometimes incorporating external partners.
- In close partnership with the Clinical Project Leaders (CPLs) of the programs, drive the process of developing and implementing the integrated strategic and operational plans for global drug development programs.
- Through leadership of the global early program team (EPT), in partnership with project team leaders and functional leaders, define project strategies, develop and maintain integrated project plans, and manage diverse teams across sites to meet project timelines and goals
- Lead project teams with respect to timing, scenario/options development, risk management, opportunities/challenges, and requirements of collaborating with Decision Boards.
- Ensure realistic resource forecasts for timelines and budget with timely communication of forecast variations and supporting rationale
- Use drug development expertise to integrate knowledge and planning of all line functions for the project
- Provide scientific experience, clinical knowledge, and indication expertise to build valuable opportunities to improve the value of existing projects and programs
- Ensure effective, proactive, and open communication within and outside the project teams in order to meet stakeholder requirements and achieve visibility and clarity of program goals, progress and issues
- Build and maintain effective and impactful teams passionate about effective cross functional communication, decision-making and resolving issues
- Strengthen the collaboration with development and commercial colleagues to champion timely transition of programs
- Act as liaison with alliance partners and thought leaders external to the company
- Participate in non-program related activities, initiatives and interfaces
The pay range for this position at commencement of employment is expected to be between $151,200 and $226,800 / year; however, while salary ranges are effective from 1/1/24 through 12/31/24, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
**Essential Requirements**:
- Masters or Doctorate in life sciences or MBA with Bachelor Degree in life science
- 5+ years pharma or biotech industry experience
- 5+ years of equivalent cross-functional leadership experience and experience leading multiple teams simultaneously
- Previous track record of success in working with global multidisciplinary drug discovery and development teams
- Excellent project / program management skills
**Desirable Requirements**:
- Expert knowledge in oncology research or drug development (including early and late-stage development) preferred but not required
Commitment to Diversity and Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Division
Biomedical Research
Business Unit
Pharma Research
Location
USA
Site
Cambridge (USA)
Company / Legal Entity
U175 (FCRS = US175) Novartis Institutes for BioMedical Research, Inc.
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
-
Global Proposal Director
5 days ago
Cambridge, United States Abt Global Inc. Full timeAbt Global Inc. Global Proposal Director Cambridge , Massachusetts Apply Now Solving the world’s most pressing issues and improving the quality of life for people worldwide is what we do every day at Abt Global. Creating a more equitable world is no small task, but we are driven by big challenges. We are a team of 3,000+ people in over 50 countries working...
-
Cambridge, United States Scholar Rock Full timeScholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the...
-
Cambridge, United States Scholar Rock Full timeScholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGF?) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the...
-
Cambridge, United States Scholar Rock Full timeScholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the...
-
Programs Summer Associate
24 hours ago
Cambridge, United States ACL Digital Full timePrograms Summer Associate #HUJP00009252Cambridge MA 0213803 Months contract with possible Extn. Note:Hybrid Remote – Tuesdays, Wednesdays and Thursdays in the office 35 hours per week. Top 3 technical or soft skills: Some research experience, worked with undergraduate students in the past, excellent writing, editing, and proofreading skills with careful...
-
Programs Summer Associate
21 minutes ago
Cambridge, United States ACL Digital Full timePrograms Summer Associate #HUJP00009252Cambridge MA 0213803 Months contract with possible Extn. Note:Hybrid Remote – Tuesdays, Wednesdays and Thursdays in the office 35 hours per week. Top 3 technical or soft skills: Some research experience, worked with undergraduate students in the past, excellent writing, editing, and proofreading skills with careful...
-
Associate Director, Global Sourcing
5 days ago
Cambridge, United States Alnylam Full timeWork_Category - hybrid Description This Associate Director role in the Global Strategic Sourcing function will be responsible for managing the Travel, Meetings and Events programs globally for the company. This includes assessment of the current programs, developing and implementing plans for improvement, and monitoring progress.This role will have...
-
Cambridge, United States Novartis Full time**Summary**: **About the Role**: **Your key responsibilities**: - Lead project teams with respect to the timing, scenario/options development, risk management, opportunities / challenges, and requirements of interfacing with Decision Boards. - Partner with project team leaders and functional leaders to define project strategies, develop and maintain...
-
Global Medical Director, Lupus
6 days ago
Cambridge, United States Biogen Idec Full timeCompany DescriptionJob Description About This Role The Global Medical Affairs Director, Lupus will be a strategic partner providing expert medical leadership to guide development, launch planning, and support for our Lupus program to improve meaningful patient outcomes. As a key member of the Lupus Global Medical Director office team reporting to the...
-
Global Medical Director, Lupus
7 days ago
Cambridge, United States Biogen Full timeAbout This Role The Global Medical Affairs Director, Lupus will be a strategic partner providing expert medical leadership to guide development, launch planning, and support for our Lupus program to improve meaningful patient outcomes. As a key member of the Lupus Global Medical Director office team reporting to the Global Medical Pipeline Head, the...
-
Global Medical Director, Lupus
5 days ago
Cambridge, United States Biogen Full timeJob DescriptionJob DescriptionJob DescriptionAbout This RoleThe Global Medical Affairs Director, Lupus will be a strategic partner providing expert medical leadership to guide development, launch planning, and support for our Lupus program to improve meaningful patient outcomes. As a key member of the Lupus Global Medical Director office team reporting to...
-
Global Medical Director, Lupus
5 days ago
Cambridge, United States Biogen Full timeJob DescriptionJob DescriptionJob DescriptionAbout This RoleThe Global Medical Affairs Director, Lupus will be a strategic partner providing expert medical leadership to guide development, launch planning, and support for our Lupus program to improve meaningful patient outcomes. As a key member of the Lupus Global Medical Director office team reporting to...
-
Global Medical Director, Lupus
6 days ago
Cambridge, United States Biogen Full timeCompany DescriptionJob DescriptionAbout This RoleThe Global Medical Affairs Director, Lupus will be a strategic partner providing expert medical leadership to guide development, launch planning, and support for our Lupus program to improve meaningful patient outcomes. As a key member of the Lupus Global Medical Director office team reporting to the Global...
-
Cambridge, United States MOMA Therapeutics Full timeMOMA Therapeutics is looking for an experienced Associate Director/Director, CMC Program Leadership Imagine joining a company where you…. * Will be part of an experienced and resilient team that is collectively unstoppable, trusts one another, and selflessly collaborates* Will work with incredible humans who are committed to the discovery of transformative...
-
Director, Global Payroll
6 hours ago
Cambridge, United States KAYAK Full time**As an employee of KAYAK, you will be part of a global network that includes OpenTable and KAYAK's portfolio of metasearch brands including Swoodoo, checkfelix, momondo, Cheapflights, Mundi and HotelsCombined. Many employees are dedicated to one brand, but we all have the benefit of using each others strengths and insights. Together, we're able to help...
-
Cambridge, United States MOMA Therapeutics Full timeMOMA Therapeutics is looking for an experienced Associate Director/Director, CMC Program LeadershipImagine joining a company where you.... Will be part of an experienced and resilient team that is collectively unstoppable, trusts one another, and selflessly collaborates Will work with incredible humans who are committed to the discovery of transformative...
-
Cambridge, Massachusetts, United States Moderna, Inc. Full timeThe Role:Moderna Therapeutics is seeking an Assoc. Director of Regulatory Labeling to support current and existing programs to be based in its Cambridge headquarters. This is a newly created role intended for a forward-looking, creative regulatory professional able to anticipate and address the challenges involved in swiftly delivering labeling for products...
-
Cambridge, United States Moderna, Inc. Full timeThe Role:Moderna Therapeutics is seeking an Assoc. Director of Regulatory Labeling to support current and existing programs to be based in its Cambridge headquarters. This is a newly created role intended for a forward-looking, creative regulatory professional able to anticipate and address the challenges involved in swiftly delivering labeling for products...
-
Associate Medical Director, Drug Safety
6 days ago
Cambridge, United States Biogen Idec Full timeCompany DescriptionJob Description What you'll do: The Associate Medical Director, Global Safety Physician will be responsible for global pharmacovigilance for investigational and/or marketed products, including review and analysis of safety data, design of clinical trials, identification and investigation of safety signals, management of benefit-risk...
-
MSP Program Director
4 days ago
cambridge, United States Randstad Enterprise Full timeThe MSP Program Director will drive profitable growth for a large managed services program; identify and drive strategic initiatives; provide operational direction and guidance to ensure consistent delivery of contract terms and KPIs; management of P&L; high level client relationship management; team management; account growth and identification of...
