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Assoc. Scientific Director, Translational Medicine- San Diego based

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.

What We Do:

Neurocrine Biosciences is 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, visit neurocrine.com, and follow the company on LinkedInX and Facebook. (*in collaboration with AbbVie)

About the Role:

Collaborate with cross functional teams to evaluate therapeutic targets, build translatable biomarker strategies, and establish robust clinical development plans. Lead clinical biomarker efforts through vendor selection, method development/validation, integration into clinical protocols, execution of sample testing at CROs, and biomarker data analysis/interpretation. The individual will have a strong strategic role on project teams responsible for translating preclinical research into clinical programs through influencing IND data packages, interacting with the FDA/EMA, building relationships with KOLs.

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

  • Establishes translational plans for designated programs and participate with senior management to align biomarker strategies to program goals to enable data-driven decisions

  • Provides disease biology expertise to clinical study teams and functional areas such as regulatory, clinical development, and clinical operations

  • Provides input to study design, protocol concepts/protocols preparation, statistical analysis plans, and reporting within assigned programs to yield high value mechanistic insight for future critical decisions

  • Collaborates with external opinion leaders. internal clinicians, research scientists and clinical operations to ensure appropriate biomarkers are incorporated within clinical studies validated appropriately for their intended use

  • Support identification and development of novel biomarker platforms

  • Engage with CROs to develop and validate clinical biomarker assays in a fit-for-purpose manner

  • Manages clinical biomarker data delivery and analysis and associated timelines by working with relevant internal functions and CROs

  • Reviews and interprets scientific knowledge of competitor landscape (molecule / indication)

  • Participate with team members to prepare abstracts, manuscripts, and presentations for external meetings as well as author biomarker sections of regulatory documents (IB, IND sections)

  • Remains up-to-date with current information on biomarker regulations, guidelines, and practices and therapeutic area knowledge and ensures consistent best practice across all activities

  • Other duties as assigned

Requirements:

  • BS/BA degree in Biology, Chemistry, or related science field and 8+ years of relevant experience OR

  • Master’s in Biology, Chemistry, or related science field and 6+ years of related experience OR

  • PharmD or PhD and 5+ years of related experience

  • Experience in immunoassay development and GxP-based biomarker platform deployment

  • Working knowledge of FDA guidance on bioanalytical method validation and related regulatory aspects

  • Understanding of biomarker assay validation and lab certification levels to support the intended purpose of clinical assay

  • Strong grasp of FDA’s BEST resource with specific knowledge around surrogate endpoints

  • Extensive experience working with CROs to support clinical assay development and sample testing

  • Excellent communication and presentation skills

  • Experience with regulatory filings and interactions

  • Demonstrated expertise in Translational Science

  • Passion and tenacity to advance patient-focused research

  • Strong knowledge of several areas within experimental medicine and biomarker development with deep expertise in at least one area

  • Ability to work effectively in cross-functional teams

  • Skill in evaluating data and data quality from multiple sources

  • Capable of making data-driven decisions that impact project/program success

  • Recognized as an emerging thought leader with technical expertise in the field

#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.

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The annual base salary we reasonably expect to pay is $170,100.00-$246,150.00. 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.

Average salary estimate

$208125 / YEARLY (est.)
min
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$170100K
$246150K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Assoc. Scientific Director, Translational Medicine- San Diego based, Neurocrine Biosciences

At Neurocrine Biosciences, we are on the lookout for an Associate Scientific Director in Translational Medicine to join our vibrant team in sunny San Diego. If you’re someone who thrives in collaboration and has a passion for transforming scientific insight into real-world therapies, this might be the perfect role for you! As an Associate Scientific Director, you will spearhead innovative biomarker strategies and clinical development plans, working directly with cross-functional teams. Your work will include evaluating therapeutic targets and leading clinical biomarker initiatives, ensuring that our findings are not just theoretical but practically applicable in bringing much-needed relief to patients suffering from neurological disorders. Imagine being at the frontline of treatments that are game-changers in areas like tardive dyskinesia and hormone-related diseases! You’ll engage with thought leaders, influence interactions with regulatory bodies like the FDA/EMA, and ensure our biomarker assays are cutting-edge and reliable. Your contributions will truly make a difference as you translate preclinical research into robust clinical programs that can impact lives. If you have a strong foundation in biological sciences and experience in biomarker development, you’ll find that your expertise is highly valued here. Join us at Neurocrine Biosciences, where your passion meets purpose, and help us continue our journey toward breakthrough discoveries that ease suffering for those in need.

Frequently Asked Questions (FAQs) for Assoc. Scientific Director, Translational Medicine- San Diego based Role at Neurocrine Biosciences
What are the responsibilities of the Associate Scientific Director at Neurocrine Biosciences?

The Associate Scientific Director at Neurocrine Biosciences plays a key role by establishing translational plans, leading biomarker strategies, and collaborating with clinical teams. This includes providing expertise in disease biology, managing data analysis, engaging with external partners, and ensuring that biomarker assays are appropriately validated. The director is also responsible for preparing regulatory documentation and publications, making this role vital in our mission to develop patient-focused research.

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What qualifications do I need to apply for the Associate Scientific Director position at Neurocrine Biosciences?

To apply for the Associate Scientific Director role at Neurocrine Biosciences, candidates should hold a BS/BA in Biology, Chemistry, or a related field with at least 8 years of relevant experience, or a Master’s with 6 years, or a PharmD/PhD with 5 years. Experience in immunoassay development, familiarity with FDA guidelines, and demonstrable expertise in Translational Science are crucial to succeed.

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Is previous experience with CROs required for the Associate Scientific Director position at Neurocrine Biosciences?

Yes, experience working with Contract Research Organizations (CROs) is essential for the Associate Scientific Director role. Candidates should have extensive experience overseeing clinical assay development and sample testing, ensuring that all processes align with current regulatory standards and practices.

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What is the salary range for the Associate Scientific Director in Translational Medicine at Neurocrine Biosciences?

At Neurocrine Biosciences, the anticipated salary range for the Associate Scientific Director position stands between $170,100.00 and $246,150.00, depending on factors such as experience and location. Additionally, this position includes a 30% annual bonus target and options for participation in equity-based incentive programs, making it a competitive package overall.

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What kind of company culture can I expect at Neurocrine Biosciences as an Associate Scientific Director?

Neurocrine Biosciences prides itself on an inclusive and positive company culture. As an Associate Scientific Director, you'll be part of a passionate team dedicated to advancements in neuroscience. The focus here is on collaboration, mutual respect, and shared values, all aimed at fulfilling our mission to relieve suffering for those in need. Personal growth and career development are strongly encouraged.

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Common Interview Questions for Assoc. Scientific Director, Translational Medicine- San Diego based
Can you describe your experience with biomarker assay development for the Associate Scientific Director role?

When discussing your experience with biomarker assay development, be specific about the types of assays you have worked on, the methodologies used, and the scientific rationale behind your approach. Highlight your familiarity with regulations, such as FDA guidance, and any successful collaborations with CROs to demonstrate your ability to lead such initiatives.

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How have you successfully translated preclinical research into clinical programs in your past roles?

To answer this, provide a concrete example of how you took preclinical findings and influenced their development into a clinical program. Detail your methodology, including collaboration with teams, data integration, and adjustments made based on findings. Convey the impact on patients or product pipelines to illustrate your effectiveness in this area.

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What strategies do you use to keep up-to-date with biomarker regulations and guidelines?

Discuss how you actively engage with scientific literature, attend relevant conferences, and participate in professional societies. You may also mention how networking with KOLs and collaborating with regulatory experts allows you to remain informed about changes in biomarker regulations and standards.

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How would you approach building relationships with external scientific partners?

Building relationships with scientific partners can be approached through regular communication, sharing mutual goals, and transparency in collaboration efforts. Mention the importance of establishing a rapport and trust and possibly give an example of successful partnerships you fostered in the past.

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What challenges have you faced when validating biomarker assays, and how did you overcome them?

Share specific challenges you encountered, such as technical difficulties or regulatory hurdles, and explain your strategic approach to resolving these issues. Highlight adaptability and persistence as key traits, showcasing your problem-solving abilities while ensuring compliance with regulatory standards.

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Describe your approach to data analysis and quality assessment for clinical biomarker data.

Discuss your systematic approach to data analysis, including tools and methodologies you have used. Emphasize your attention to detail in evaluating data quality and integrity and how this has influenced critical decisions in past projects.

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How do you ensure your translational plans are aligned with overall program goals?

Explain how you collaborate with senior management and cross-functional teams to develop translational plans. Emphasize the importance of understanding program goals and ensuring all biomarker strategies are directly relevant to these objectives to drive data-informed decisions.

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What motivates you to work in the field of neuroscience and translational medicine?

Share your personal connection to neuroscience or mention specific experiences that have fueled your motivation. Discuss your passion for improving patient outcomes and how this aligns with Neurocrine Biosciences' mission to relieve suffering.

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Can you give an example of how you’ve contributed to a regulatory submission?

Provide specific details about your role in a regulatory submission, emphasizing your contributions to preparing necessary documentation, ensuring compliance, and collaborating with regulatory agencies. This could include submitting IND sections or biomarker data that played a crucial role in the submission process.

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What personal qualities do you think are essential for an Associate Scientific Director?

Discuss qualities such as leadership, communication skills, strategic thinking, and a deep commitment to scientific integrity and patient care. You could also mention adaptability and resilience as critical traits for navigating the dynamic nature of translational medicine.

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