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About Company

We are looking for an experienced clinical data manager to join our team. You will be responsible for managing the clinical trial data for our pharmaceutical, biotechnology, and medical device company. The ideal candidate should have a solid understanding of clinical data management principles, regulatory guidelines, and industry best practices. You will work independently and with cross-functional teams to ensure timely and accurate data delivery.

Position Name :

Clinical Data Management Intern

Organization :

Pride Circle


B.Pharma or M.Pharma




₹300k - ₹600k/year



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.


  • 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.