Clinical Contracts Manager

At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.

Neurocrine Biosciencesis a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, 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 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, visitneurocrine.com, and follow the company onLinkedIn,XandFacebook. (*in collaboration with AbbVie)

About the Role:

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• Join our team as a vital contributor in the exciting world of clinical operations. Your key responsibilities will include spearheading the negotiation of pivotal clinical trial contracts, meticulously managing the end-to-end processing of contracts within project timelines and providing invaluable operational support across a spectrum of projects and vendors. As our go-to expert for outsourced studies, you will skillfully oversee CRO contracts and budget agreements, acting as a linchpin between CROs, legal entities, and clinical operations departments.

• In addition to these critical functions, you will play a pivotal role in crafting Clinical Trial Agreement templates and budget grids, streamlining the CTA start-up process, and collaborating closely with regulatory bodies to ensure a seamless execution of contracts. Your expertise will be vital in negotiating budgets with clinical sites, closely collaborating with finance teams, and ensuring timely payments in alignment with contract terms.

• As a seasoned professional in the domain, you will share your wealth of knowledge by mentoring junior team members on complex clinical accounting and administrative contract duties. While embracing the dynamic nature of the role, you will also actively contribute to shaping and refining contracting processes, showcasing your prowess in both leadership and innovation.

• Ready to make a tangible impact in the fast-paced realm of clinical operations? Come aboard and be part of a team that values your expertise, fosters growth, and champions excellence in every aspect of your role. Your journey with us begins here - are you ready to elevate your career to new heights?

• 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

• Knowledge of Clinical Trial process, regulations and guidelines

• Ability to work effectively across a matrix organization

• Ability to prepare/negotiate external provider master service agreements, work/change orders, etc. and track for clinical operations

• Ability to read and interpret contracts, ensure contract language / terms meet company standards

• Strong contract administration skills, including budgeting, billing/invoicing, issue resolution, point of contact for CRO

• Knowledge of clinical contract accounting and budgeting process

• Solid understanding of drug development and clinical operations

• Has knowledge of best practices in the functional discipline and familiarity with the broader underlying concepts of related business disciplines

• Works to improve tools and processes within functional area

• Developing reputation inside the company as it relates to area of expertise

• Ability to work as part of and lead multiple teams

• Exhibits leadership skill and ability, typically leads lower levels and/or indirect teams

• Excellent computer skills

• Excellent communications, problem-solving, analytical thinking skills

• Sees broader picture, impact on multiple departments/divisions

• Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency

• Excellent project management and organizational skills

• Excellent interpersonal and communication skills and experience supporting multiple teams

• Strategic thinker who is able to identify issues and improve processes

• Ability to work effectively across a matrix organization

• Advanced knowledge in Microsoft Word and Excel

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Neurocrine Biosciences is an EEO/AA/Disability/Vets employer.

We are committed to building a diverse, equitable, and inclusive workplace, 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.

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