Clinical Research Data Analyst (Pharm D or M Pharm)

Overview

Job Title: Clinical Research Data Analyst

Job Type: Full-Time, Hybrid

Job Responsibilities

• Review patient records sourced from various Electronic Health Record (EHR) systems, adhering to provided eligibility criteria, and adeptly map eligible patients with appropriate clinical studies.
• Prepare comprehensive summaries of reviewed patient records and provide detailed reports on assigned charts.
• Actively participate in knowledge transfer sessions related to therapeutic areas, contributing to internal knowledge development.
• Demonstrate flexibility in managing multiple studies, prioritizing tasks, and shifting between projects as needed.
• Contribute to the development and refinement of clinical trial protocols and guidelines as needed.

Job Requirements

• Pharm D or M Pharm degree with 6 months to 1 year of relevant experience in CRO, Clinical Pharmacy, Medical Coding, Scientific writing or a related domain.
• Strong understanding of clinical research methodologies, regulatory requirements, and ICH-GCP guidelines.
• Ability to interpret complex clinical data, troubleshoot operational challenges, and deliver actionable insights.
• Proficiency in Microsoft Office Suite (Excel, PowerPoint, Word).
• Strong understanding of medical terminologies, MedDRA, biostatistics, SAS, and/or R.
• Familiarity with CTMS platforms (Medidata, Oracle Clinical, Veeva Vault).
• Strong written and verbal communication skills to document findings and liaise with cross-functional teams.
• Flexibility to adapt to evolving project demands and reallocate focus as necessary.

Job Type: Full-time

Schedule:

• Day shift

Application Question(s):

• Notice period to join

Language:

• English (Preferred)

Work Location: In person