Contracts Manager (Prolaio)

Posted 4 Days Ago
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Chicago, IL, USA
In-Office
100K-130K Annually
Senior level
Biotech
The Role
Manage Prolaio’s complete contract lifecycle, including drafting, reviewing, negotiating, processing, execution, renewals, and terminations. Oversee contract intake, obligations, deadlines, reporting, compliance, risk escalation, and CLM processes. Serve as a liaison to business stakeholders, vendors, consultants, clinical sites, and collaboration partners. Support process improvements, strategic contracting initiatives, training, and broader Legal Department projects.
Summary Generated by Built In

About Us 

Kardigan is a heart health company working to make cardiovascular disease preventable, curable and no longer the leading cause of death in the world.
It is Kardigan’s mission to develop multiple targeted treatments in parallel that bring people with cardiovascular diseases to the cures they deserve.
 
Led by Tassos Gianakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D., Kardigan’s co-founders have reunited after leading MyoKardia to discover and develop mavacamten, the first cardiac myosin inhibitor, resulting in an acquisition by Bristol Myers Squibb in 2020.
 
We have a cutting-edge discovery and translational research platform, a pipeline of late-stage candidates, and an industry-leading team that is driven to improve the lives of patients.
 
At Kardigan, we are motivated by our values which guide how we work, interact, and achieve our goals. Driven by patients and their families, we are deeply committed to improving the lives of patients and prioritizing their needs above all else. We believe in being authentic—leading with truth to bring out the best in others by creating an environment where every person knows they will be fully accepted. With an eagerness to learn, we encourage the highest levels of curiosity and are open to changing our minds. We are committed to winning as a team with urgency, excellence, and intention, and support each other no matter what role we play or where we sit. Lastly, we strive to enable the impossible because patients are counting on us. We are not afraid to take risks to unlock innovation and advance scientific discoveries.
 
These values are the foundation of our work, empowering us to make a real difference, every day.
 
 
Prolaio is seeking an experienced Contracts Manager whose primary role will be to manage the complete contract lifecycle for Prolaio, including all aspects of contract creation, processing, drafting and administration for Prolaio.  Employed by Kardigan and embedded within Prolaio, this role will support other initiatives, projects and programs within the broader Legal Department as requested.  We are seeking an exceptional candidate with strong contract administration experience and attention to detail, who can collaborate cross-functionally, negotiate agreements, and communicate clearly and effectively. Attention to detail is essential in this role. You will join our fast-paced legal team, reporting to our Vice President, Corporate Law. This is a highly visible position within the companies as you will interface directly with business stakeholders and leadership.
 
Position Title: Manager, Contracts
Department: Legal 
Reports To: VP, Corporate Law
Location: Chicago, IL - Hybrid Model (2-3 days a week) 

Essential Duties and Responsibilities:

  • Contract Lifecycle Management
    • Independently draft, review, and negotiate a broad range of contracts including service agreements, consulting agreements, NDAs, vendor and supplier contracts, and statements of work (SOWs).
    • Translate business needs into clear, legally sound contract language, balancing risk mitigation with operational flexibility.
    • Ensure contractual terms comply with applicable laws, company policies, and industry regulations.
    • Assist with the implementation of a contract lifecycle management (CLM) tool).
    • Track key contractual obligations, renewals, and deadlines.
    • Identify, assess, and escalate legal and business risks when necessary.
    • Drive collaboration with a wide range of internal and external stakeholders, including vendors, service providers, consultants, clinical sites, and collaboration partners.
  • Contract Operations & Reporting
    • Manage contracts and process form requests from intake to execution and track Manage contracts from intake to execution, tracking status and communicating risks, priorities, and solutions to stakeholders at all levels.
    • Develop and prepare key performance metrics and generate periodic reports on contract management.
    • Coordinate and manage execution, renewals, and terminations of contracts.
    • Drive continuous improvement initiatives to optimize contracting processes, workflows, operational efficiency, and cross-functional alignment.
  • Business Partnership & Training
    • Serve as the primary liaison for internal partners and stakeholders on contract negotiations, processes, and operations, including anticipating contracting needs and providing guidance.
    • Partner with senior business leaders and cross-functional stakeholders to support strategic contracting initiatives and organizational priorities.
  • General
    • Monitor contract-related activities for compliance with internal policies, industry regulations, and applicable laws.
    • Support special projects and contract-related initiatives.
    • Perform other duties as requested, including initiatives supporting the broader Kardigan Legal Department.

Qualifications and Preferred Skills

  • Bachelor's degree preferred; Paralegal certification preferred.
  • At least 7 years of relevant experience with a minimum of 5 years of contract administration within the pharmaceutical, life sciences, or medical device industry.
  • Proven excellence in contract drafting and negotiation, with a solid foundation in biotech/pharma/med device contract terms and best practices, and the ability to manage complex agreements independently.
  • Proficient in contract lifecycle and procurement processes, including experience with contract lifecycle management systems, e-signature platforms, and collaboration platforms; previous CLM implementation and administration experience strongly preferred.
  • Strong organizational and planning skills with the ability to triage, prioritize, and effectively advance multiple simultaneous projects in a fast-paced environment.
  • Excellent issue spotting, problem-solving, and communication skills, with the ability to collaborate with individuals at all levels inside and outside the organization.
  • Skilled in Microsoft Office Suite, PowerPoint, SharePoint, Excel, and Adobe Acrobat.
  • Commitment to integrity, ethical conduct, and handling confidential information with discretion.
  • Meticulous attention to detail; able to work independently with good judgment and a strong team-oriented mindset.

Exact Compensation may vary based on skills, experience and location.

Pay range

Exact Compensation may vary based on skills, experience and location.

Pay range
$100,000—$130,000 USD

Skills Required

  • Bachelor's degree
  • Paralegal certification
  • At least 7 years of relevant experience
  • At least 5 years of contract administration experience within the pharmaceutical, life sciences, or medical device industry
  • Experience independently drafting and negotiating complex agreements
  • Knowledge of biotech, pharmaceutical, or medical device contract terms and best practices
  • Proficiency with contract lifecycle and procurement processes
  • Experience with contract lifecycle management systems, e-signature platforms, and collaboration platforms
  • Previous contract lifecycle management implementation and administration experience
  • Strong organizational and planning skills, including prioritizing multiple simultaneous projects
  • Excellent issue-spotting, problem-solving, and communication skills
  • Proficiency with Microsoft Office Suite, PowerPoint, SharePoint, Excel, and Adobe Acrobat
  • Ability to handle confidential information with discretion and demonstrate ethical conduct
  • Meticulous attention to detail and ability to work independently with sound judgment

Kardigan Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Kardigan and has not been reviewed or approved by Kardigan.

  • Healthcare Strength — Comprehensive medical, dental, and vision coverage is paired with life and disability insurance and an EAP, signaling a robust core benefits backbone. Employer materials present this coverage as part of a standard, well-rounded package for a U.S. biotech.
  • Fair & Transparent Compensation — Explicit salary ranges are posted for multiple roles and the company highlights competitive salaries, indicating greater pay transparency for candidates. The careers site and job postings also outline an annual bonus program, clarifying elements of total cash compensation.
  • Leave & Time Off Breadth — Paid holidays and paid time off are called out, with culture materials referencing “generous” PTO. These signals point to substantive time-off provisions even if accrual details are not yet specified.

Kardigan Insights

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The Company
HQ: Princeton, NJ
56 Employees
Year Founded: 2023

What We Do

Kardigan is a patient-driven heart health company that is modernizing cardiovascular drug development to deliver medicines that move patients beyond symptom management to functional cures. By matching critical disease drivers with treatment responders identified in clinical trials, Kardigan is developing a portfolio of medicines that modify the underlying cardiovascular disease pathophysiology to get patients closer to the cures they deserve. For more information about Kardigan, please visit kardigan.bio. If you are interested in joining our passionate and driven team with deep cardiovascular, biotechnology and operational expertise, please visit kardigan.bio or the careers tab of this page.

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