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    Associate Specialist, Document - San Diego, United States - Neurocrine Biosciences

    Neurocrine Biosciences
    Neurocrine Biosciences San Diego, United States

    3 weeks ago

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    Description
    Who We Are:

    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, but few options.

    What We Do:

    Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple 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. *in collaboration with AbbVie

    About the Role:
    The TMF Document & Clinical System Associate Specialist provides operational support and maintenance for clinical systems including an Electronic Trial Master File (eTMF) and Clinical Trial Management System (CTMS). Assists in the coordination of documentation associated with conducting clinical studies. Assist Clinical Operations (CO) Study Teams and Functional Groups with management of the TMF documents, SOPs and record archiving. The TMF Document & Clinical Systems Associate/Specialist may be responsible for serve as a resource during internal or external audits and regulatory inspections of the TMF.

    Your Contributions (include, but are not limited to):
    • Perform data entry and reconciliation in various clinical systems and tracking tools
    • Perform secondary quality check (QC) for documents submitted to the TMF
    • Provides support to study team including, but not limited to, maintenance of documentation, clinical tracking and information retrieval.
    • Assist with the organization of the controlled clinical document storage on-site
    • Assists with off-site archiving activities (including cataloguing process and document retrieval).
    • Assist the Sr. Specialist with documenting the set-up, review, maintenance and archival of study specific TMFs in TMF Plans and study specific TMF Index. Plans may include TMF transition and/or migration activities
    • Work with study team to ensure "inspection readiness" at all times
    • Perform additional tasks and duties as assigned
    Requirements:
    • BS/BA degree in life science or related field or RN and with some relevant experience working directly with clinical trial documentation working at a biotech/pharmaceutical company or CRO OR
    • High School diploma and Minimum of 4 years of clinical support experience with essential regulatory documents
    • Working knowledge of clinical study documents and managing Trial Master Files in Clinical Systems (eTMF and CTMS - Veeva preferred)
    • Ability to process, archive, and retrieve documents in electronic format
    • Working knowledge of clinical trials
    • Good computer skills
    • Understands Neurocrine's business objectives and develops understanding of Neurocrine's services and customers
    • Has experience in specific functional discipline while working to acquire higher-level knowledge and skills
    • Comfortable with tools and processes that support work conducted by functional area
    • Ability to work as part of a team
    • Strong computer skills
    • Good interpersonal, organizational, communications, problem-solving, analytical thinking skills
    • Detail oriented
    • Ability to meet deadlines
    • Good project management skills
    #LI-TM1

    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.

    The hourly rate we reasonably expect to pay is $33.98-$48.01. 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 15% 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.
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