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.
