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Clinical Data Manager /Data Analyst (Remote)

Penfield Search Partners
Fairfield, CT

Quick Apply

Job Details

Contract

Qualifications

Data-driven problem-solving

Full Job Description

Contact: Neisha Camacho/Terra Parsons - [email protected]
No 3rd party candidates

We are partnering with a growing biotech organization seeking a Clinical Data Manager/Data Analyst to support ongoing and upcoming clinical programs across multiple therapeutic areas.

This role will sit within a highly collaborative clinical development team and is ideal for a hands-on, analytical Clinical Data Manager who enjoys digging into the data, identifying trends or issues proactively, and developing creative solutions to improve data quality and study execution. The client is seeking someone resourceful and technically curious — not just process-oriented — with the ability to independently explore datasets, generate meaningful reports, and surface potential issues early.

The ideal candidate will bring a blend of traditional clinical data management expertise along with strong data review, querying, and analytical skills. Experience with R, SQL, SAS, or other data interrogation and reporting tools is highly desirable.

Key Responsibilities

Support clinical data management activities across studies from start-up through database lock
Perform hands-on data review and exploratory analysis to identify data trends, inconsistencies, missing data patterns, and potential study risks
Develop custom reports, listings, and data visualizations to support proactive data cleaning and study oversight
Utilize R, SQL, SAS, or similar tools to query, analyze, and troubleshoot clinical datasets
Partner with CROs and vendors to ensure high-quality, timely data delivery
Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical, and Safety teams on data review strategies and issue resolution
Contribute to development and review of key deliverables including:
- Data Management Plans (DMPs)
- eCRF design and completion guidelines
- Edit checks and query logic
- User Acceptance Testing (UAT)
- Data review plans and cleaning processes
Support ongoing query management and ensure data integrity, consistency, and inspection readiness
Assist with implementation of data standards, reporting enhancements, and process improvements
Work independently to investigate data anomalies and recommend practical solutions in a fast-paced biotech environment

Qualifications

BS in a scientific, technical, or clinical discipline
Approximately 5–8 years of clinical data management experience within biotech, pharma, or CRO environments
Strong hands-on experience reviewing and interrogating clinical trial data
Experience using R, SQL, SAS, or other querying/reporting tools to analyze clinical data and generate custom reports
Experience with EDC systems such as Medidata Rave, Oracle, or Veeva
Working knowledge of CDISC standards (SDTM/ADaM) and downstream data usage
Experience supporting Phase II and/or III clinical trials; CNS experience is a plus
Exposure to CRO/vendor oversight
Understanding of clinical data structures and dictionaries including MedDRA and WHODrug
Strong critical thinking and problem-solving skills with the ability to work independently
Resourceful, proactive, detail-oriented, and comfortable operating in a dynamic biotech environment
Strong communication and cross-functional collaboration skills

Quick Apply

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