Senior Clinical Contracts Manager

Who We Are:

---------------

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients with Prader-Willi syndrome, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (**in collaboration with AbbVie*)

About the Role:

-------------------

Responsible for leading the development of clinical site budgets including review, adjustment, and negotiation with clinical sites. Interacts closely with legal department to ensure clinical contracts are fully executed in a timely manner. Manages administration / execution of clinical contracts (invoicing, timelines, issues, etc.) across multiple projects. Manages clinical contracts output, tracking and interactions with Accounting and legal teams for consistency across and within Clinical programs. May supervise contract administrators.

_

Your Contributions (include, but are not limited to):

---------------------------------------------------------

• Manages clinical trial contractual negotiations including triaging, reviewing and identifying issues for escalation across multiple projects
• Manages and ensures on-time processing of all clinical contracts from initial request through execution in accordance with the project timelines
• Attends clinical operational meetings as needed to advise on clinical contracting activities across multiple projects and vendors
• For studies that are outsourced, manages CRO contracts, site and budget agreement activities and serves as a primary contact and budget liaison between CRO, company legal and clinical operations
• Oversees the CTA start-up process. Development and routing of CTA templates, budget grids and supporting documentation sent to sites. Serves as escalation contact with sites for contracts. Submits web requests and coordinates with Legal Department on execution of CTAs
• Collaborates with Head of Clinical Operations (or designee) in managing work orders, service agreements, consulting agreements, license agreements, MSAs and CDAs
• Oversees and guides budget negotiation with clinical sites based on parameters defined by Head of Clinical Operations (or designee)
• Collaborates with finance/accounting departments in support of contract budgets and monthly/quarterly reviews
• Manages invoices associated with clinical trials and ensures payments are made based on executed contracts
• Contributes to process efficiencies and organization of contracting and budget/payment processes
• Mentors and appropriately delegates/collaborates cross functionally on assignments for growth of direct reports
• Leads onboarding process for clinical contracts personnel
• Other duties as assigned

Requirements:

-----------------

• BS/BA degree in business administration or health care/science related field AND 8\+ years of experience in a CRO, Biotech or Pharmaceutical organization. Experience with contract management, negotiation, budgeting and administration including billing/invoicing, issue resolution, point of contact for CRO. OR
• Master's degree in business administration or health care/science related field AND 6\+ years of similar experience noted above
• Anticipates business and industry issues; recommends relevant process / technical / service improvements
• Demonstrates broad expertise or unique knowledge
• Considered an expert within the company and may have external presence in area of expertise
• Applies in-depth expertise in discipline and broad knowledge of other closely related areas to improve efficiency of team
• Ability to work as part of and lead multiple teams
• Good leadership, mentoring skills and abilities typically leads lower levels and/or indirect teams
• Excellent computer skills
• Excellent communications, problem-solving, analytical thinking skills
• Sees broader picture and longer-term impact on division/company
• Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency
• Excellent project management, strong project leadership skills
• Expert at managing complexity and multiple work streams in changing circumstances
• Advanced knowledge of Clinical Trial process, regulations and guidelines
• Proven success working effectively across a matrix organization.
• Demonstrated ability to prepare/negotiate external provider master service agreements, work/change orders, etc. and track for clinical operations
• Ability to read and interpret highly complex, variety of clinical contracts, ensure contract language / terms meet company standards.
• Expert contract administration skills, including managing budgets, billing/invoicing process, issues through resolution, act as point of contact for CRO(s)
• Advanced knowledge of clinical contract accounting and budgeting process
• Advanced understanding of drug development and clinical operations

#LI-SA1

Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don’t line up to exactly what we have outlined in the job description.

_

The annual base salary we reasonably expect to pay is $148,500\.00-$203,000\.00\. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.