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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Data Management, ensuring data integrity and compliance with Good Clinical Practices (GCP). Proven leadership in managing teams and driving project timelines while maintaining high-quality standards.

Highest-signal resume keywords

Clinical Data ManagementLeadership and Team ManagementGood Clinical Practices (GCP)Data Review and Quality ControlProject Documentation and Reporting

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

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

Tools & Technologies

Microsoft Office

Industry Keywords

Clinical ResearchHealth SciencesBiological SciencesMathematical SciencesStandard Operating ProceduresBusiness Practices

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