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BioForum

Senior Clinical Data Specialist

BioForum

Senior Clinical Data Specialist at Bioforum India managing data for clinical trials in Bangalore. Leading a team, ensuring quality, and driving timelines in a hybrid environment.

Posted 7/5/2026full-timeBangalore • 🇮🇳 IndiaSeniorWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Demonstrate strong work ethic, commitment, and a commitment to quality
  • Foster a cohesive and motivated data management team
  • Supervise and lead Clinical Data Specialists
  • Support the Clinical Data Strategy Lead in driving timelines and deliveries
  • Coordinate data reviews by assigning tasks and responsibilities to team members
  • Ensure adherence to established Business Practices, Standard Operating Procedures, and Working Instructions
  • Review study specific protocols and provide input in the design of eCRF
  • Lead and direct the development and implementation of Data Cleaning Listings
  • Actively contribute to the development of the study specific Data Management documentation
  • Independently oversee data reviews for studies
  • Serve as escalation point for unresolved data issues
  • Pro-actively identify and manage risks on assigned projects
  • Support with holistic data reviews and provide insights on Data Trends, Risks and Anomalies
  • Maintain accurate and up-to-date project documentation
  • Generate project-related reports and metrics to monitor project performance
  • Ensure timely and appropriate filing of all Data Management project documentation
  • Ensure clinical trial data completeness, integrity, and consistency
  • Implement and execute robust quality control procedures

Requirements

What you’ll need
  • Bachelor’s degree (or equivalent education) in health, clinical, biological, or mathematical sciences, or a related field
  • 6+ years of experience in the clinical research industry
  • 4 years proven expertise in data management
  • Proficient in English
  • Strong communication and collaboration aptitude
  • Strong administrative skills (Planning, organizing, time management etc.)
  • Excellent skills in Data Management
  • Proven leadership and team management skills
  • Proven skills in establishing and maintaining effective working relationships
  • Good problem-solving skills
  • Strong attention to detail
  • Proficient in Microsoft Office products
  • Proven technical abilities
  • Knowledge of the clinical trial process flow
  • Excellent understanding of Good Clinical Practices (GCP)

Benefits

Comp & perks
  • Health insurance
  • Professional development
  • Flexible work arrangements

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
Data ManagementData Cleaning ListingsECRF DesignClinical Trial Process FlowProject Performance MetricsRisk ManagementData Trends AnalysisTechnical AbilitiesQuality Control Procedures
Soft Skills
Strong CommunicationCollaboration AptitudeProblem-Solving SkillsAttention to DetailAdministrative Skills