Principal Specialist, Clinical Data Mgmt
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Before you apply
Salary$131k – $179k
LocationUS MA Home Office
Work moderemote · United States
Typefull-time
SeniorityLead
Experience3+ yrs
EquityIncluded
Company size1,001–5,000 people
PostedSep 17, 2026 · 1mo ago
Verified live4d ago
At a glanceSummarised by Seekless from the posting.
BS/BA degree in computer science or a related discipline AND 8+ years of experience in the Pharmaceutical Industry
Master's degree in computer science or a related discipline AND 6+ years of similar experience
PhD in computer science or a related discipline AND 4+ years of similar experience
3+ years of experience serving in a supervisory or lead capacity
Thorough understanding of the drug development process
Experience working with GCP and CDISC/CDASH/SDTM standards
Developing SOPs/Work Instructions, and following required FDA guidance documents
Hands-on clinical database programming skills, including SAS, SQL, and Medidata Rave Architect
Ability to communicate effectively both verbally and in writing
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
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 communication, 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 skills
Experience with Business Objects, Rave Targeted SDV and Batch Uploader
Experience with C# programming (custom functions)
EEO/Disability/Vets employer
Skills
SAS
SQL
Medidata Rave Architect
Business Objects
Rave Targeted SDV
Batch Uploader
C#
CDISC
CDASH
SDTM
MedDRA
WHO Drug dictionary
Benefits
Retirement savings plan
Paid vacation
Paid holiday
Paid personal days
Paid caregiver leave
Paid parental leave
Paid medical leave
Medical insurance
Prescription drug insurance
Dental insurance
Vision insurance
Annual bonus
Equity based long term incentive
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 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:
Leads, performs, and oversees data management activities for assigned clinical studies for both in-house and outsourced clinical trial data; evaluates, develops, and implements data management processes, procedures, and tools to ensure business requirements are met; collaborates within Biometrics and with Medical, DSPV, Regulatory, QC, and other internal customers to ensure high quality data in support of regulatory submissions, safety reporting, and publications.
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Your Contributions (include, but are not limited to):
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Leads, performs, and oversees data management activities for clinical studies and/or clinical programs
•
Experience leading and supporting First-In-Human (FIH) clinical studies, including early protocol review, eCRF and database design, and alignment with dose-escalation and safety objectives
•
Hands-on management of data management activities for FIH studies, with emphasis on rapid data cleaning, near real-time safety data review, and support for frequent interim analyses
•
Close collaboration with Clinical Operations, Safety, and Biostatistics teams to support timely decision-making and governance in FIH studies
•
Performs hands-on clinical data management tasks to support clinical studies, including, but not limited to: reviewing study protocols, designing eCRFs, performing and coordinating user acceptance testing (UAT), documenting edit check specifications, QC’ing external data transfers, performing data quality checks/discrepancy review, and ensuring database lock activities are completed
•
Participate in, review, and lead development of policies, Standard Operating Procedures (SOPs), processes, and associated documents for data management; provide input on SOPs and processes in which data management is involved
•
Promote/advocate data management at inter- and intradepartmental meetings
•
Provide technical expertise to staff within Data Management, Biometrics, and other NBI departments; develop and execute training, including project-specific training, as necessary
•
Assist with responding to questions and findings from QA audits; ensure responses to Corrective Action Forms (CAFs) are closed out appropriately
•
Actively research current industry trends and share information with appropriate individuals at NBI
•
Recommend improvements to existing data management practices and procedures, including identifying, recommending, and implementing solutions for technology issues
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Assist in the development of standardized documents within data management (both within and across projects/programs), including electronic case report forms and edit checks
•
Oversee screening, selection, validation, and implementation of data management software purchases and upgrades
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Participate in selecting outsourcing vendors and review data management sections of proposals, including scope of work; monitor budgets as appropriate
•
Coordinate data management timelines for individual projects and well as clinical programs, including database lock, DSMB meetings, data review meetings, and monitoring CRO performance of data management tasks to ensure that timelines are met and that any resource issues are identified and resolved
•
Monitor in-house resources of assigned projects and identify potential deficiencies; work with supervisor to develop and implement a plan to overcome any obstacles
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Ensure that appropriate quality control checks and audit procedures are implemented according to department SOPs
•
Run data review listings, issue queries, code Medical History and AE data using MedDRA dictionary and code Concomitant Medications using WHO Drug dictionary
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Collaborate with database programmer to ensure NBI database standards, including CDISC/SDTM, are followed for both in-house and, if appropriate, outsourced projects
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Identify areas of risk and proactively communicate issues and solutions to supervisor and/or appropriate colleagues and team members
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Actively participate in data management-related NDA submission activities, as appropriate
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Provide feedback, as requested, for performance evaluations. Identify strengths and areas for improvement for DM team members and work with supervisor to create a plan to develop team members
•
Perform other duties as assigned
Requirements:
•
BS/BA degree in computer science or a related discipline AND 8+ years of experience in the Pharmaceutical Industry, (either in-house/sponsor or CRO). OR
•
Master’s degree in computer science or a related discipline AND 6+ years of similar experience noted above OR
•
PhD in computer science or a related discipline AND 4+ years of similar experience noted above OR
•
3+ years of experience serving in a supervisory or lead capacity
•
Qualified candidate must have a thorough understanding of the drug development process
•
Experience working with GCP and CDISC/CDASH/SDTM standards
•
Developing SOPs/Work Instructions, and following required FDA guidance documents
•
Must have hands-on clinical database programming skills, including SAS, SQL, and Medidata Rave Architect
•
Experience with Business Objects, Rave Targeted SDV and Batch Uploader preferred.
•
Experience with C# programming (custom functions) is a plus
•
Ability to communicate effectively both verbally and in writing
•
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
•
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 communication, 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 skills
Legal
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.
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Benefits
The annual base salary we reasonably expect to pay is $130,800.00-$179,000.00. 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.