Cliniminds Noida Adv PGD Clinical Research CDM SAS FAQs
Ques. What EDC platforms are covered in this full-time CDM and SAS programme?
Ans. The programme provides hands-on training in Medidata Rave and Oracle Clinical, the two leading Electronic Data Capture systems in clinical trials globally. Candidates learn database build, edit check programming, audit trail review, data cleaning workflows, CDISC SDTM mapping, data lock, and unblinding procedures applicable to Phase I through Phase III clinical trial operations at pharmaceutical companies and CROs across India.
Ques. How does the full-time format differ from part-time CDM programmes at Cliniminds?
Ans. The full-time format provides daily classroom engagement at the Noida centre, allowing candidates to complete the comprehensive clinical research, CDM, and SAS curriculum within six months through structured practical sessions and intensive EDC and SAS exercises. The part-time format covers similar content over a longer timeline and suits working professionals who cannot commit to full-time study schedules.
Ques. Which CDISC standards are taught and how are they applied in SAS programming?
Ans. The curriculum covers CDISC CDASH for case report form standards, CDISC SDTM for regulatory submission domains (DM, AE, LB, VS, EX, MH), and CDISC ADaM for analysis datasets (ADSL, ADAE, ADLB). SAS programming is taught specifically for SDTM mapping, ADaM dataset creation, and regulatory submission preparation for FDA NDA and EMA MAA clinical trial applications.
Ques. What career roles can graduates of this full-time programme pursue?
Ans. Graduates typically pursue roles such as Clinical Data Manager, SAS Programmer (Clinical), Database Programmer, Clinical Research Coordinator, CDISC Mapping Specialist, and Regulatory Submissions Analyst at pharmaceutical companies, Contract Research Organisations, and clinical data management service providers across India and globally in the life sciences industry.
Ques. Is an internship or industry project included in this full-time programme?
Ans. Cliniminds incorporates practical project work and case study simulations using real clinical trial data in this full-time programme. Candidates should contact Cliniminds directly at cliniminds.com to confirm current details of any internship partnerships with pharma companies or CROs applicable to the specific batch they plan to join at the Noida centre.
Ques. Is prior clinical research or CDM experience required for admission?
Ans. No prior experience is required. A Bachelor’s degree in life sciences, pharmacy, nursing, or a related field with minimum 50% marks is the primary eligibility criterion. The full-time programme takes fresh graduates through foundational to advanced clinical research, CDM, and SAS competencies within six months of intensive training at Cliniminds Noida, Sector 62.







Comments