Global clinical research organization (CRO) Quanticate has announced an exciting opportunity for aspiring clinical research professionals. The company is currently hiring a Clinical Data Coordinator I in Bengaluru, Karnataka. This role offers candidates the opportunity to work on global clinical trials, support clinical data management activities, and contribute to the development of life-changing therapies.

Professionals with experience in Clinical Data Management (CDM), Oracle Clinical, Medidata Rave, Inform, and ICH-GCP guidelines are encouraged to apply for this promising healthcare and clinical research career opportunity.

About Quanticate

Quanticate is a leading data-focused Contract Research Organization (CRO) specializing in statistical programming, biostatistics, and clinical data management services. The company partners with top pharmaceutical companies and emerging biotechnology firms worldwide, helping deliver high-quality clinical research solutions.

Job Details

Key Responsibilities

The selected candidate will be responsible for supporting clinical data management activities across multiple studies, including:

• Assisting with study database testing and validation before activation.
• Preparing study-specific documentation and materials.
• Processing and reviewing clinical trial data for completeness and accuracy.
• Reviewing Case Report Forms (CRFs) against Data Management Plans.
• Raising and resolving data queries.
• Managing Data Clarification Forms (DCFs).
• Performing quality control checks on clinical databases and CRFs.
• Supporting study documentation archiving and project closeout activities.
• Conducting medical coding activities when assigned.
• Collaborating with project managers, sponsors, investigators, and global teams.
• Identifying opportunities for process improvements and quality enhancement.

Required Qualifications

Candidates applying for the Clinical Data Coordinator job at Quanticate should possess:

Knowledge Requirements

• Strong understanding of Clinical Data Management processes.
• Knowledge of ICH-GCP guidelines and regulatory requirements.
• Familiarity with CRO and sponsor-driven study standards.

Experience Requirements

• Previous experience in Clinical Data Management or a related role.
• Hands-on experience with clinical data management systems such as:
  • Oracle Clinical
  • Medidata Rave
  • Inform
• Experience supporting multiple clinical studies is preferred.

Skills Required

• Excellent attention to detail.
• Strong analytical and problem-solving abilities.
• Effective written and verbal communication skills.
• Strong organizational and time management capabilities.
• Proficiency in Microsoft Word and Excel.
• Ability to work in fast-paced, deadline-driven environments.
• Team collaboration and stakeholder management skills.

Benefits Offered by Quanticate

Employees joining Quanticate can expect:

• Competitive salary package.
• Flexible working hours.
• Annual leave, sick leave, and casual leave.
• Medical insurance for employees and immediate family members.
• Gratuity benefits.
• Accidental insurance coverage.
• Professional development programs.
• Mentoring and coaching opportunities.
• E-learning and job shadowing initiatives.
• Exposure to international clinical research projects.

Why Consider This Clinical Data Management Job?

The Clinical Data Coordinator I position provides valuable exposure to end-to-end clinical trial data management processes. Candidates will gain practical experience in database testing, query management, CRF review, medical coding, and regulatory compliance while working alongside global pharmaceutical and biotechnology clients.

This role is ideal for professionals looking to build a long-term career in:

• Clinical Data Management
• Clinical Research
• Pharmacovigilance
• Regulatory Affairs
• Biostatistics
• Clinical Operations

How to Apply

Application Link