Senior Clinical Data Manager

This is a fully remote position, open to applicants in India.

📋 Description

• Plan and execute the establishment, programming, and ongoing upkeep of data management systems for clinical research initiatives.

• Ensure research data is complete, accurate, and of high quality for final analysis.

• Assume project management responsibilities for assigned initiatives when appropriate.

• Collaborate with Research Fellows, Division Heads, Project Managers, and external stakeholders to identify data collection and reporting needs.

• Design or assist in the design of electronic data collection systems.

• Design or assist in creating Case Report Forms and other data collection instruments.

• Maintain data collection systems effectively.

• Engage in the development and validation of new data management systems and processes.

• Create and generate data reports.

• Mentor, train, and oversee data management personnel.

• Strategize project plans and allocate resources accordingly.

• Work collaboratively with clinical, programming, statistics, and other project team members.

• Lead or take part in special projects aimed at enhancing processes, tools, systems, and organizational efficiency.

• Complete and attend mandatory training sessions.

• Take part in objective setting, performance management, role assessments, and career development activities.

• Participate in project management, organizational meetings, and workshops.

• Adhere to regulations, guidelines, SOPs, project requirements, and pertinent systems.

• Execute quality control and report or escalate any risks and issues.

• Contribute to internal meetings, continuous improvement initiatives, knowledge sharing, and staff development.

• Comply with Work Health and Safety legislation and practices.

⛳️ Requirements

• Tertiary qualifications in science or a related field.

• 10–12 years of progressively responsible experience in data coordination for clinical trials.

• Strong IT skills, encompassing SQL, reporting software, all Microsoft Office applications, web-based databases, and internet usage.

• Strong conceptual ability to quickly learn new software applications.

• Experience with statistical packages is desirable but not mandatory.

• Demonstrated capability to manage large data sets, including reporting and evaluation procedures.

• Solid understanding of relevant Good Clinical Practice, NHMRC, and TGA regulatory guidelines, particularly concerning data quality and accuracy.

• Ability to assess and recommend improvements to existing processes and procedures.

• Exceptional time management and project management abilities.

• Excellent written and verbal communication skills.

• Advanced problem-solving, analytical, and strategic thinking skills.

• Strong interpersonal skills with the ability to work flexibly, independently, in small teams, and with diverse stakeholders, including senior management.

• Proficiency in Microsoft Office packages.

• Ability to maintain focus on both strategic context and detail/quality.

• Flexibility and adaptability in dynamic and ambiguous environments.

🏝️ Benefits

• Purpose-driven work that contributes to clinical trials in renal, cardiometabolic, and oncology therapies.

• Competitive compensation with a customized salary and benefits package.

• Hybrid or remote working arrangements based on location and role.

• Opportunities for learning and access to a global network of scientific leaders.

• Employee wellbeing programs that promote work-life balance, health, and team cohesion.

• Participation in global engagement surveys.

• Recognition programs.

• Team-building events.

• Exposure to diverse international projects and clients.