×
Register Here to Apply for Jobs or Post Jobs. X
More jobs:

Associate Director Data Management

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Acadia Pharmaceuticals
Full Time position
Listed on 2026-02-18
Job specializations:
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

About Acadia Pharmaceuticals

Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs.

At Acadia, we’re here to be their difference.

Please note that this position is based in San Diego, CA. Acadia's hybrid model requires this role to work in our office three days per week on average.

Position Summary

The Associate Director will collaborate with the Data Management team by providing leadership and knowledge. Assists the head of Data Management in directing the design, documentation, testing and implementation of clinical data collection studies, and clinical database reviews in support of company objectives. Ensures that the data management systems are business ready and of appropriate quality to fulfill those objectives. Focuses on the oversight of quality data deliverables within Acadia Data Management and projects with Contract Research Organizations (CROs).

Primary

Responsibilities
  • Participates in the collaboration and coordination with others to design and implement clinical protocols and data collection systems.
  • Assists in identifying and resolving data management issues on assigned studies.
  • Responsible for ensuring data management timelines are met within assigned studies, in-house or outsourced.
  • Provides strategic input into protocol design focused on data management portions.
  • May assist Biostatistics in development/review of Statistical Analysis Plans.
  • Reviews and resolves data discrepancies for standardized data validation systems and procedures, when applicable.
  • Supports data management requirements and deliverables for New Drug Application (NDA)/Marketing Authorisation Application (MAA), including integrated databases.
  • Aids in production of quality data deliverables to support regulatory submissions, publications and due diligence activities.
  • Reviews clinical, regulatory and other documents, as needed, to assure data integrity and quality.
  • Oversees projects that have been engaged with CROs, as well leads and manages internal projects.
  • Oversees and manages final data management electronic Trial Master File (eTMF) for assigned studies.
  • Assists with the development of standards and process documentation, including Standard Operating Procedures and Work Instructions.
  • Assures compliance with industry quality standards, guidelines and procedures.
  • Assists in the selection and evaluation of new personnel to ensure the efficient operation of the function.
  • May assist in the career development of Data Management personnel. Position may have direct reports. May assist with input into corporate and department budget process and management.
  • Other responsibilities as assigned.
Education and Experience
  • Bachelor’s degree in Life Sciences, Mathematics or related field. Targeting 8 years of progressively responsible experience within the pharmaceutical, biotech or CRO industry. An equivalent combination of relevant education and experience may be considered.
  • Previous experience in data management from protocol concept through database lock and clinical study report finalization.
  • Knowledge of medical terminology.
  • Knowledge of coding dictionaries (Medical Dictionary for Regulatory Activities - MedDRA, WHO Drug).
  • Excellent verbal and written communication skills as well as interpersonal and organizational skills
  • Proficiency in MS Office applications.
  • Proficiency with data management systems and supporting statistical programs (e.g., SAS).
  • Knowledge of database design and database concepts.
  • Skilled at cross-functional/department communications to gain cooperation of others.
  • Proven skill at effectively leading a cooperative team effort and organizing resources to achieve team goals.
  • Able to make and…
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary