Job Description
Job Title: Clinical Data Management (CDM)
Role Responsibilities
• Oversee the full lifecycle of clinical data management processes.
• Ensure the quality and integrity of clinical trial data.
• Develop and implement data management plans.
• Monitor data entry and validation processes.
• Coordinate with clinical teams to ensure timely data collection.
• Conduct data cleaning and review activities.
• Prepare data for statistical analysis and reporting.
• Ensure compliance with regulatory requirements and industry standards.
• Participate in protocol development and study design.
• Utilize data management software for efficient data handling.
• Facilitate communication between project stakeholders.
• Identify and resolve data discrepancies in a timely manner.
• Provide training and support to junior data management staff.
• Generate data visualization and reports for project updates.
• Collaborate with cross-functional teams to streamline processes.
Qualifications
• Bachelor's or Master’s degree in Life Sciences or related field.
• 10 years of experience in clinical data management.
• Proven experience with data management software and tools.
• Strong understanding of clinical trial methodologies.
• Excellent analytical and problem-solving skills.
• Knowledge of regulatory guidelines (ICH-GCP, FDA).
• Familiarity with statistical software (SAS, SPSS) is preferred.
• Detail-oriented with a high level of accuracy.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Project management experience is a plus.
• Proficient in MS Office Suite (Excel, Word, PowerPoint).
• Ability to manage multiple projects with competing priorities.
• Willingness to work on-site in India.
• Professional certification in Clinical Data Management is a plus.
• Strong organizational skills and ability to meet deadlines.
Skills: ms office suite (excel, word, powerpoint),clinical data management,organizational skills,data visualization,database management,interpersonal skills,regulatory guidelines (ich-gcp, fda),statistical software (sas, spss),analytical skills,communication skills,data cleaning and validation,statistical analysis,problem-solving skills,clinical data,regulatory compliance,cdm,rave,data validation,quality assurance,data management software,crf design,project management
Role Responsibilities
• Oversee the full lifecycle of clinical data management processes.
• Ensure the quality and integrity of clinical trial data.
• Develop and implement data management plans.
• Monitor data entry and validation processes.
• Coordinate with clinical teams to ensure timely data collection.
• Conduct data cleaning and review activities.
• Prepare data for statistical analysis and reporting.
• Ensure compliance with regulatory requirements and industry standards.
• Participate in protocol development and study design.
• Utilize data management software for efficient data handling.
• Facilitate communication between project stakeholders.
• Identify and resolve data discrepancies in a timely manner.
• Provide training and support to junior data management staff.
• Generate data visualization and reports for project updates.
• Collaborate with cross-functional teams to streamline processes.
Qualifications
• Bachelor's or Master’s degree in Life Sciences or related field.
• 10 years of experience in clinical data management.
• Proven experience with data management software and tools.
• Strong understanding of clinical trial methodologies.
• Excellent analytical and problem-solving skills.
• Knowledge of regulatory guidelines (ICH-GCP, FDA).
• Familiarity with statistical software (SAS, SPSS) is preferred.
• Detail-oriented with a high level of accuracy.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Project management experience is a plus.
• Proficient in MS Office Suite (Excel, Word, PowerPoint).
• Ability to manage multiple projects with competing priorities.
• Willingness to work on-site in India.
• Professional certification in Clinical Data Management is a plus.
• Strong organizational skills and ability to meet deadlines.
Skills: ms office suite (excel, word, powerpoint),clinical data management,organizational skills,data visualization,database management,interpersonal skills,regulatory guidelines (ich-gcp, fda),statistical software (sas, spss),analytical skills,communication skills,data cleaning and validation,statistical analysis,problem-solving skills,clinical data,regulatory compliance,cdm,rave,data validation,quality assurance,data management software,crf design,project management
💡 Quick Summary
Seeking a career-building opportunity? The Clinical Data Management(CDM) position is now open for candidates interested in the Database Administrator sector. This role in Bangalore offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Database Administrator is a plus.
