Clinical Data Manager I – Clinical Data Management Jobs in Bengaluru | Quanticate Careers India
Company: Quanticate
Job Title: Clinical Data Manager I
Location: Bengaluru
Department: Clinical Data Management
Employment Type: Full-Time
Work Mode: On-Site
Experience Required: 6–8 Years
Industry: CRO | Clinical Research | Pharmaceutical Industry | Clinical Trials
About Quanticate
Quanticate is a globally recognized data-focused Contract Research Organization (CRO) specializing in Clinical Data Management, Biostatistics, Statistical Programming, and Clinical Trial Support Services. The organization partners with leading global pharmaceutical companies and emerging biotech firms to deliver high-quality clinical development solutions.
Quanticate is known for handling complex global clinical trials requiring advanced clinical data management expertise, regulatory compliance, and high-level project leadership.
Job Overview – Clinical Data Manager I
Quanticate is hiring experienced professionals for the position of Clinical Data Manager I in Bengaluru, India. This role is ideal for candidates with strong expertise in Clinical Data Management (CDM), study leadership, project coordination, and regulatory compliance within the CRO or pharmaceutical sector.
The selected candidate will lead and manage end-to-end Clinical Data Management activities throughout the lifecycle of clinical studies while ensuring quality, accuracy, compliance, and timely project delivery.
Key Responsibilities
Clinical Data Management Operations
Lead and coordinate all Clinical Data Management activities from study initiation to database lock.
Ensure delivery of CDM procedures as per contractual agreements, SOPs, ICH-GCP guidelines, and regulatory standards.
Maintain consistency, quality, and compliance across multiple clinical projects.
Manage Case Report Forms (CRFs) and all related CDM activities.
Perform medical coding activities when assigned.
Support development and review of internal SOPs and CDM strategies.
Stay updated with the latest advancements in Clinical Data Management systems and industry trends.
Project Management Responsibilities
Plan and manage study timelines, deliverables, and project resources.
Monitor project progress and communicate updates to management teams.
Coordinate project activities across multiple CDM functions.
Ensure successful study execution and timely completion of milestones.
Team Management & Leadership
Allocate projects and responsibilities in collaboration with Project Management teams.
Support training, mentoring, and professional development of team members.
Conduct performance evaluations when required.
Manage assigned direct reports and ensure efficient task delivery.
Client & Stakeholder Management
Act as the primary Clinical Data Management contact for internal and external stakeholders.
Coordinate with data processing and programming teams for project execution.
Build and maintain strong client relationships within clinical research projects.
Eligibility Criteria
Educational Qualification
Bachelor’s Degree or higher in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related healthcare disciplines preferred.
Experience Required
6–8 years of experience in Clinical Data Management within a CRO or pharmaceutical organization.
Prior experience in leading clinical studies is mandatory.
Required Skills & Technical Expertise
Clinical Data Management Skills
Strong expertise in end-to-end Clinical Data Management processes
Study leadership and project management experience
CRF management and clinical database oversight
Medical coding knowledge
CDM Systems Knowledge
Candidates should possess hands-on experience with at least two Clinical Data Management platforms such as:
Oracle Clinical
Medidata Rave
INFORM
Regulatory & Compliance Knowledge
Strong understanding of ICH Guidelines and GCP
Knowledge of global clinical trial regulations and data handling standards
Familiarity with pharmaceutical industry compliance requirements
Soft Skills
Excellent communication and stakeholder management skills
Strong leadership and team coordination abilities
Client relationship management expertise
Problem-solving and analytical thinking capabilities
Why Join Quanticate?
Working with Quanticate provides professionals the opportunity to contribute to global clinical research programs while building long-term careers in Clinical Data Management and Clinical Research Operations.
The organization actively promotes employee growth through:
Mentoring and coaching programs
E-learning and job shadowing opportunities
Professional development initiatives
Exposure to global pharmaceutical and biotech projects
Employee Benefits
Competitive salary package based on experience
Flexible working hours
Annual Leave, Sick Leave, Casual Leave, and Bank Holidays
Medical Insurance for employees and immediate family members
Gratuity benefits
Accidental insurance coverage
Career development and learning opportunities
Important Recruitment Notice
Quanticate does not request payments, deposits, or paid training/course fees during any stage of the recruitment process. All official communication is conducted only through authorized company email domains.
Apply for Clinical Data Management Jobs in Bengaluru
Professionals seeking advanced opportunities in:
Clinical Data Management Jobs
CRO Careers in India
Medidata Rave Jobs
Oracle Clinical Jobs
Clinical Research Careers
Pharma Data Management Roles
CDM Project Lead Jobs
can apply for this exciting opportunity with Quanticate in Bengaluru, Karnataka, India.
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