Job Openings
Senior Clinical Data Manager
About the job Senior Clinical Data Manager
Job Title: Senior Clinical Data Manager
Job Location: India
Job Location Type: Hybrid
Job Contract Type: Full-time
Job Seniority Level: Mid-Senior level
At Emerald Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.
Our therapeutic expertise spans renal, cardiometabolic, and oncology—areas where we make a significant impact on improving global health.
At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.
About The Role
The Senior Clinical Data Manager is responsible for planning and implementing the set-up, programming and ongoing maintenance of data management systems in support of Emerald Clinical research projects to ensure the collection of complete and accurate data for final analysis.
Your Responsibilities
Key Accountabilities
Ensuring quality and accuracy of research data
Where appropriate, take on project management role for assigned projects
Liaison with project staff (Research Fellows, Division Heads, Project Managers, external parties) to determine data collection and reporting requirements
Designing, or assisting in the design of electronic data collection systems
Designing, or assisting in the design of Case Report Forms or other data collection tools
Maintaining systems for data collection
Participate in the development and validation of new data management systems and processes as necessary.
Designing and generating data reports
Mentor, train and supervise data management staff
Project planning and planning resources
Interact with clinical, programming and statistics project leads and other project team members
Personal Development
Lead/participate in special projects to continuously improve processes, tools, systems and organization.
Mandatory attendance at core training.
Participate in objective setting, performance management, review of the position and the planning and implementation of personal and career development activities.
Actively participate in project management, organizational meetings and workshops.
Demonstrate understanding and adherence to the organization values.
Training, Quality and Compliance
Complete mandatory training for this role within specified timelines
Attend mandatory training sessions required for this role
Identify resources and training to support learning and development within this role
Comply with all applicable regulations, guidelines, SOPs and project-specific requirements Comply with all designated systems relevant to this role
Ensure own quality control of all relevant processes and activities performed
Report and escalate identified risks and issues in areas of responsibility according to Emerald Clinical and/or project requirements
Customer Focus and Teamwork
Attend and actively participate in Emerald Clinical meetings and other internal meetings and activities as required
Provide input to systems, tools and processes to support continuous improvement
Share knowledge with others, to facilitate learning and development across the organization
Work Health and Safety
Comply with Work Health & Safety (WH&S) legislation and operate in accordance with established organizational WH&S practice and procedures
Promote and contribute to a safe, secure environment for staff and visitors
About You
Tertiary qualifications in science or related field
10 – 12years of increasing responsibility in data coordination of clinical trials.
Strong IT skills including SQL, reporting software, all MS Office applications, web-based databases and the Internet, and strong conceptual ability to learn new software applications quickly.
Experience With Statistical Packages Is Desired But Not Essential.
Proven ability to handle large data sets, including reporting and other evaluation procedures
A strong understanding of relevant Good Clinical Practice, NHMRC and TGA regulatory guidelines, especially as connected with data quality and accuracy
Ability to evaluate and recommend changes to existing processes and procedures for greater effectiveness
Competencies
Excellent time management and project management skills
Excellent written and verbal communication skills
Ability to see the big picture yet still focus on detail and quality of work.
Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments
Why Join Us?
At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.
Here’s What Makes Us Stand Out
We understand that great work happens when people feel valued and supported. That’s why we provide:
We are an equal-opportunity employer and encourage applications from all qualified candidates.
Our therapeutic expertise spans renal, cardiometabolic, and oncology—areas where we make a significant impact on improving global health.
At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.
About The Role
The Senior Clinical Data Manager is responsible for planning and implementing the set-up, programming and ongoing maintenance of data management systems in support of Emerald Clinical research projects to ensure the collection of complete and accurate data for final analysis.
Your Responsibilities
Key Accountabilities
Ensuring quality and accuracy of research data
Where appropriate, take on project management role for assigned projects
Liaison with project staff (Research Fellows, Division Heads, Project Managers, external parties) to determine data collection and reporting requirements
Designing, or assisting in the design of electronic data collection systems
Designing, or assisting in the design of Case Report Forms or other data collection tools
Maintaining systems for data collection
Participate in the development and validation of new data management systems and processes as necessary.
Designing and generating data reports
Mentor, train and supervise data management staff
Project planning and planning resources
Interact with clinical, programming and statistics project leads and other project team members
Personal Development
Lead/participate in special projects to continuously improve processes, tools, systems and organization.
Mandatory attendance at core training.
Participate in objective setting, performance management, review of the position and the planning and implementation of personal and career development activities.
Actively participate in project management, organizational meetings and workshops.
Demonstrate understanding and adherence to the organization values.
Training, Quality and Compliance
Complete mandatory training for this role within specified timelines
Attend mandatory training sessions required for this role
Identify resources and training to support learning and development within this role
Comply with all applicable regulations, guidelines, SOPs and project-specific requirements Comply with all designated systems relevant to this role
Ensure own quality control of all relevant processes and activities performed
Report and escalate identified risks and issues in areas of responsibility according to Emerald Clinical and/or project requirements
Customer Focus and Teamwork
Attend and actively participate in Emerald Clinical meetings and other internal meetings and activities as required
Provide input to systems, tools and processes to support continuous improvement
Share knowledge with others, to facilitate learning and development across the organization
Work Health and Safety
Comply with Work Health & Safety (WH&S) legislation and operate in accordance with established organizational WH&S practice and procedures
Promote and contribute to a safe, secure environment for staff and visitors
About You
Tertiary qualifications in science or related field
10 – 12years of increasing responsibility in data coordination of clinical trials.
Strong IT skills including SQL, reporting software, all MS Office applications, web-based databases and the Internet, and strong conceptual ability to learn new software applications quickly.
Experience With Statistical Packages Is Desired But Not Essential.
Proven ability to handle large data sets, including reporting and other evaluation procedures
A strong understanding of relevant Good Clinical Practice, NHMRC and TGA regulatory guidelines, especially as connected with data quality and accuracy
Ability to evaluate and recommend changes to existing processes and procedures for greater effectiveness
Competencies
Excellent time management and project management skills
Excellent written and verbal communication skills
- High level problem solving, analytical, and strategic thinking skills
Ability to see the big picture yet still focus on detail and quality of work.
Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments
Why Join Us?
At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.
Here’s What Makes Us Stand Out
- Purpose-Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
- Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
- Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.
We understand that great work happens when people feel valued and supported. That’s why we provide:
- Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
- Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
- Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
- Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
- Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.
We are an equal-opportunity employer and encourage applications from all qualified candidates.
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