Job summary
Job post source
This job is directly from Neurocrine Biosciences
Job overview
The Clinical Site, Contracts Manager at Neurocrine Biosciences manages clinical site contract lifecycle and budget negotiations to support timely study startups and clinical operations.
Responsibilities and impact
The role involves negotiating and managing clinical site contracts, collaborating with clinical research sites, leading contract startup processes, coordinating with legal and finance teams, managing site payments, improving contracting processes, and mentoring team members.
Compensation and benefits
The position offers an annual base salary range of $117,300 to $170,050, a 30% target annual bonus, equity-based long-term incentives, retirement savings with company match, paid leave, and comprehensive health benefits including medical, dental, and vision coverage.
Experience and skills
Candidates need a BS/BA with 6+ years or a Master's with 4+ years in CRO, biotech, or pharma, with contract management, negotiation, budgeting, and clinical trial knowledge; strong leadership, communication, project management, and analytical skills are required.
Career development
The job provides opportunities to develop expertise in clinical site contracting, lead teams, improve processes, and gain a reputation within the company in this functional area.
Work environment and culture
Neurocrine Biosciences emphasizes a strong, inclusive, and positive culture focused on purpose and values, fostering belonging, respect, and empowerment.
Company information
Neurocrine Biosciences is a neuroscience-focused biopharmaceutical company dedicated to developing treatments for neurological and neuropsychiatric disorders with a diverse portfolio and robust clinical pipeline.
Unique job features
This role uniquely combines contract lifecycle management with clinical operations, offering leadership in contract negotiations and site budget management within a leading biotech company.
Company overview
Neurocrine Biosciences is a biopharmaceutical company focused on developing treatments for neurological and endocrine-related disorders. They generate revenue through the commercialization of their FDA-approved drugs, including Ingrezza for tardive dyskinesia and Orilissa for endometriosis pain, in collaboration with AbbVie. Founded in 1992, the company has a rich history of innovation, marked by its commitment to addressing unmet medical needs through cutting-edge research and development.
How to land this job
Position your resume to highlight expertise in clinical site contract lifecycle management, emphasizing skills in budget negotiation, contract execution, and collaboration with clinical teams and legal departments.
Focus on showcasing your ability to manage multiple clinical site contracts, including CDAs, CTAs, amendments, and payment processes, while demonstrating strong project management and organizational skills.
Apply through multiple platforms such as Neurocrine Biosciences' official corporate careers page, LinkedIn, and reputable job boards to maximize your application visibility.
Connect with professionals in the clinical operations or site management divisions at Neurocrine Biosciences on LinkedIn; use ice breakers like commenting on recent company developments in neuroscience, asking about their experience with site contract challenges, or expressing enthusiasm for the company’s mission to relieve suffering through innovative therapies.
Optimize your resume for ATS by incorporating key terms from the job description such as 'clinical site contracts,' 'budget negotiation,' 'CTA start-up process,' 'clinical trial regulations,' and 'contract administration' to ensure your resume passes automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple submission channels, and find LinkedIn contacts for networking, enabling you to focus your time on interview preparation and skill enhancement.
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