Senior Program Manager

Asimov; United States; On-site; USD 130,000 - 180,000; Full time

Job summary

Asimov in the United States is seeking a Senior Program Manager to join our Customer Engagement team and own end-to-end success of campaigns across Biologics and Genetic Medicine. You will align with the commercial lead on account strategy and with operations on program execution to deliver clear, consistent stories for our partners.

You will synthesize feedback from multiple teams, manage cross-functional relationships, and prioritize the customer experience as an extension of their own team.

Qualifications

• Bachelor's or Master's degree in life sciences, business, or a related field.
• PM qualifications (PMP, PRINCE2, APM, or equivalent) preferred.
• 7+ years of program/project management experience in a Life Science service organization (e.g., CDMO, CRO).

Responsibilities

• Drive program delivery by tracking milestones and surfacing gating decisions.
• Coordinate cross-functionally with operations and vendor partners to keep execution aligned to plan.
• Identify risks early and communicate them to initiate preventive actions.
• Manage relationships with CDMO and third-party networks; coordinate international shipment logistics.
• Surface expansion or renewal opportunities from execution insights.

Skills

Program management

Cross-functional collaboration

Stakeholder communication

Education

Bachelor's or Master's degree in life sciences, business, or related field

Tools

Google Workspace

CRM/PSA platform

Job description

Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform--from cells to software--to enable the design and manufacture of next-generation therapeutics.

Asimov is looking for a Senior Program Manager to join our Customer Engagement team and own the end-to-end success of our campaigns for the full stack of technologies we offer across Biologics and Genetic Medicine.

This role sits at the intersection of Commercial and Operations. It means aligning with our commercial lead on account strategy and with the technical operations on program execution. We are looking for someone who is able to clearly synthesize feedback from multiple teams to build one clear, and consistent story for our partners. . The successful candidate will prioritize our customer's experience by being genuinely invested in their success and acting as an extension of their own team.

About the Role:

Delivery Execution:

• Drive program delivery by tracking milestones and surfacing gating decisions to internal and external stakeholders.
• Coordinate cross functionally with internal technical operations, and CDMO/vendor partners to keep execution aligned to plan.
• Identify technical, operational, and cost risks early and communicate them clearly to initiate preventive actions with the right groups.
• Manage relationships and track activities with CDMO and third-party vendor networks. Coordinate international shipment logistics for biological materials.
• Contribute to building scalable internal program management processes and tools as the function grows and evolves.

Commercial Partnership:

• Serve as the point of contact for program-level status, scope, and timeline, coordinating closely with the commercial lead who is responsible for the overall account relationship.
• Own the relationship between what is contracted and what's actually being delivered, flagging scope, scheduling, or cost risks before it surprises the customer or Asimov.
• Use direct visibility into execution to surface expansion, renewal or adjacent scope opportunities for the commercial lead to pursue.
• Escalate issues requiring both technical and commercial judgement, framed in terms of what it means for the program and ultimately the entire relationship with our clients.

About You:

• Bachelor's or Master's degree in life sciences, business, or a related field
• Recognized program management qualification (PMP, PRINCE2, APM, or equivalent) is preferred.
• 7+ years of program/project management experience in a Life Science service organization (e.g CDMO, CRO), with a strong understanding of cell line development and/or biologics process development.
• You have a track record of driving alignment across a matrixed organization. Earning real influence with cross-functional stakeholders (commercial, technical, and operational alike) without formal authority over them.
• You have a working understanding of R&D and CMC workflow within BioPharma.
• You're an effective communicator and have experience communicating program status and risks directly to external customers.
• You have proficiency working with structured project tracking tools and Google Workspace, etc.
• You are familiar with adjacent tooling such as a CRM or PSA platform.

We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.