Clinical Data Management Intern

Shift Type: Monday – Friday, 9 AM to 6 PM

Hiring LGBT Apprentices/Interns Only

Role: Clinical Data Management Specialist – Intern

Company: Big Pharma Company (80% employee referral rate)

Experience: Freshers only

Work Location: Bangalore

Employment: Full-time

Who Can Apply: LGBT candidates as part of a diversity hiring initiative

To Apply:
Please send CVs to pamela@thepridecircle.com if you are from the LGBT Community ONLY.

Responsibilities:

• Oversee the collection, validation, and processing of clinical trial data.
• Develop and implement data management procedures for clinical trials.
• Support and facilitate the review of medical coding for validity and completeness.
• Ensure compliance with applicable regulations, protocols, and standard operating procedures.
• Maintain high data quality standards throughout the data lifecycle.
• Stay updated on industry best practices, technological advancements, and regulatory requirements.

Daily Tasks:

• Develop and maintain data management documentation (e.g., study protocols, case report forms, data management plans).
• Design case report forms (CRFs) and electronic data capture (EDC) systems.
• Perform data entry and cleaning activities, including discrepancy management and query resolution.
• Conduct data validation checks and implement quality control measures.
• Develop and execute standard operating procedures (SOPs) for data management activities.
• Collaborate with study team members to resolve data-related issues.
• Generate and review data listings, summaries, and reports for clinical study reports.
• Ensure compliance with guidelines, Good Clinical Practice (GCP), CDISC standards, and other regulations.
• Contribute to the development and validation of data management software tools.

Required Skills and Qualifications:

• B.Pharma or M.Pharma fresher candidates.
• 0-1 years of experience in clinical data management or a similar role.
• Strong understanding of clinical trial processes and data management principles.
• Proficiency in EDC systems and clinical data management software.
• Familiarity with GCP and CDISC standards.
• Knowledge of data analysis and reporting software (e.g., SAS, SQL, Oracle Clinical).
• Excellent attention to detail with strong problem-solving and analytical skills.
• Strong organizational and time management abilities.

Preferred Skills and Qualifications:

• Certification in clinical data management (e.g., CCDM).
• Knowledge of CRF design and MS Project.
• Understanding of CDISC standards and data interchange formats (e.g., SDTM, ADaM).
• Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).
• Understanding of data privacy and protection regulations (e.g., GDPR).
• Effective communication and interpersonal skills.

To Apply:
If you are from the LGBT+ Community, please send your CV to pamela@thepridecircle.com.