CRISPR Therapeutics AG

Senior Manager, Program Management

CRISPR Therapeutics AG$140K — $155K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Degree in life sciences with 3-4+ years of program management experience or 10+ years with a bachelor's degree for senior manager role.
  • Outstanding leadership and management skills with a scientific and product development perspective.
  • Ability to thrive in a matrix environment while managing multiple tasks and priorities.
  • Proficient in project management tools and Microsoft Office suite.
  • Detailed knowledge of preclinical and early clinical product development and regulatory requirements.
  • Familiarity with cell and molecular biology techniques, particularly LNP delivery.

Responsibilities

  • Drives program operational aspects including strategy and tactical implementation plans.
  • Ensures adherence to program plans and timelines through objective setting and prioritization.
  • Facilitates alignment and support among cross-functional teams for program execution.
  • Optimizes project plans and tracks resources and time to ensure milestones are met.
  • Anticipates program risks and develops timely action plans for issue resolution.
  • Leads communication to ensure transparency of program objectives and progress to all stakeholders.
  • Represents the program to senior management, aligning it with corporate strategy.

Benefits

  • Dynamic workplace with a balance of remote work flexibility and in-person interactions.
  • Collaborative environment fostering mentorship opportunities and cross-functional communication.
Full Job Description
Job Description:

Position Summary

The successful candidate will play a critical role in achieving outcomes for our R&D programs. This person will join a strong program management team in the Boston, MA facility driving the success of R&D development teams. The individual will work collaboratively with the program teams and will manage and integrate the diverse drug development activities in key areas that include discovery, preclinical research, CMC and clinical manufacturing, regulatory affairs, clinical development, commercial, program strategy and finance.

This is an exciting and interdisciplinary role for a highly qualified and motivated individual. The successful candidate will be a confident program manager, with attention to detail and significant prior success in preclinical and early clinical stage program management for therapeutic programs in the biotechnology industry. The ideal candidate will be detail driven and have a proven track record in managing and driving program success. The successful candidate will also have a solid scientific understanding of the biology of genome editing technologies, as well as the development of cell and gene therapies. We are seeking someone with a sense of urgency for developing important new therapies for devastating diseases and who is interested in forging new and uncharted paths for patients with the exciting CRISPR technology.

Responsibilities
  • Drives program team(s) and is responsible for working closely with Program Leader and program team members to manage the operational aspects of the program(s), including developing overall strategy, tactical implementation plans, fully integrated program plan and timelines, and monitoring key milestones and decision points to drive delivery of program objectives
  • Drives team objective setting, prioritization, and tracking ensuring adherence to plan and strategy
  • Ensures cross-functional alignment and organizational support for the program plan and timelines by facilitating internal and external stakeholder management
  • Implements project plan flawlessly; optimizes and tracks progress of project plans (time, resources)
  • Interfaces and coordinates with relevant functional groups to ensure timely execution of program activities including anticipating and identifying program risks, mitigations and contingencies, and supporting timely action plans and issue resolution
  • Drives issue identification and resolution and leads contingency planning for program team
  • Ensures effective, proactive, and open communications, horizontally and vertically, in order to achieve transparency and clarity of program goals, progress, and issues, and, where necessary, engages line function management, other internal stakeholders and external experts to overcome obstacles
  • Represents program to Senior Management; ensures effective communication to align program activities with corporate strategy, and ensure effective program execution
  • Identifies and resolves conflicts at program team and functional team level
  • Fosters a culture of ownership and single point of accountability with clear timelines, as well as ongoing evaluation, recognition and process improvement
  • Is attuned to team dynamics and focuses on team needs directly and/or in partnership with other organizational leaders to ensure optimal team effectiveness
  • Focuses operations to deliver results by influencing team members beyond existing benchmarks and their own expectations
  • Leads ad-hoc cross-functional task forces and day-to-day operations of program team
  • Ensures the development and use of key program management tools including GANTT charts, and the use of management logistics and documentation, by all team members, to enhance program delivery and information dissemination to the team and key stakeholders
  • Ensures effective program team meetings, logistics and documentation
  • For programs that are in alliances, drives reporting and program management with collaboration partners


Minimum Qualifications
  • Degree in the life sciences with at least 3-4+ years of demonstrated program management experience managing cross-functional product development teams
    • Senior Manager:
      • 10+ Years of relevant experience with a bachelor's degree
      • 8+ Years of relevant experience with an advanced degree
  • Outstanding leadership and management skills with an integrated view of scientific and product development issues, and demonstrated passion for creating new medicines
  • Ability to work independently and successfully in a matrix environment, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively
  • Proficiency in project management applications (ex.MS Project, Visio, ThinkCell, MS Timeline) as well as MS Word, MS PowerPoint and MS Excel
  • Detailed understanding of preclinical and early clinical product development for biologics, and regulatory requirements for IND and CTA filings and First-In-Human clinical trials
  • Familiarity with cell and molecular biology techniques, LNP delivery
  • Strong oral and written communication skills, a high degree of energy, accuracy and attention to detail, and a passion for delivering important new medicines to patients with devastating diseases


Preferred Qualifications
  • PMP certification
  • Thorough understanding of the preclinical and early clinical development of cell and gene therapy medicines
  • Experience driving gene editing or cell & gene therapy, LNP & RNA programs
  • Advanced planning and tracking skills, capable of managing multiple projects with respect to priorities and self-management
  • Expert in Communication and Information management.
  • Expert leadership skills demonstrated in program teams, Expert skills to facilitate/ optimize contributions from team members as individuals and members of a cohesive team
  • Strong interpersonal and communication skills for bridging between scientific and business participants, for driving a program to effective implementation and for managing effective collaborations; strong verbal communication, expert in written communications, expert team player

Competencies
  • Collaborative - Openness, One Team
  • Undaunted - Fearless, Can-do attitude
  • Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit - Proactive. Ownership mindset.


CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.

Senior Manager, Program Management: Base pay range of $140,000 to $155,000+ bonus, equity and benefits

About CRISPR Therapeutics AG

CRISPR Therapeutics AG, a gene editing company, focuses on developing transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 gene-editing platform. The company develops its products through in-house research programs and partnerships with biopharmaceutical companies and academic researchers. Its lead product candidate is CTX001, an ex vivo CRISPR gene-edited therapy for treating patients suffering from transfusion-dependent beta thalassemia or severe sickle cell disease in which a patient's hematopoietic stem cells are engineered to produce high levels of fetal hemoglobin in red blood cells. The company was formerly known as Inception Genomics AG and changed its name to CRISPR Therapeutics AG in April 2014. CRISPR Therapeutics AG was founded in 2013 and is headquartered in Zug, Switzerland.
Learn more about CRISPR Therapeutics AG
Size
473 employees
Market Cap
$3.3 billion
Industry
Net Income
-$348.8 million
Founded
2013
5 Year Trend
+181.6%
Revenue
$720,000
NASDAQ

Similar Jobs

More Jobs at CRISPR Therapeutics AG

More Pharmaceuticals & Biotech Jobs

Find similar Senior Manager, Program Management jobs: