Statistical Programmer - Internship

About the internship:Note: These statements reflect the general description of the position and are not intended to be an all-inclusive list of tasks to which employee may be assigned

Selected intern's day-to-day responsibilities include:

1. Develop, validate and review SAS codes and outputs which transform raw data to CDISC, SDTM & ADaM standards.

2. Prepare and review documents related to study and CDISC package.

3. Review and provide necessary input in database design template and eCRF.

4. Identify data quality issues and communicate to respective stakeholders.

5. Maintain all necessary records for the reporting phase of the study.

6. Perform the validation of the software/programs used for analysis of statistical data.

7. Write and revise SOPs as per need and maintain awareness of and adherence to all current SOPs.

8. Conforms to training schedule for own position and maintains awareness of SOP content, according to company requirements. Who can apply:Only those candidates can apply who:are available for full time (in-office) internshipcan start the internship between 29th Sep'26 and 3rd Nov'26are available for duration of 6 monthsare from Gandhinagar onlyhave relevant skills and interests* Women wanting to start/restart their career can also apply.* Freshers looking for jobs may also applyStipend:INR₹ 12,500 - 15,000 /monthDeadline:[hidden]:59:59Other perks:Job offerSkills required:SAS and R ProgrammingAbout Company:Cliantha Research, full-service clinical research organization (CRO), provides comprehensive and integrated offerings in Early Phase (BA/BE and Phase I) trials, Late Phase (Phase II-IV) patient-based trials, Consumer Clinical Research, Bioanalytical, IVRT/IVPT , Biometrics, Medical Services, Allergy Testing - Environmental Exposure Chambers (EECs) and Veterinary Therapeutics (Preclinical-Bioanalytical). Cliantha, by leveraging on the depth of experience provides ethical, value-added customer centric services rooted in excellence, thereby enabling clinical development of pharmaceutical, biotech & healthcare companies.Cliantha has expanded its footprint to three countries, and is supported by a strong team of over 1,500 professionals. Cliantha has successfully undergone inspections by major global regulatory authorities, including the US FDA, EU (AGES, ANSM, AEMPS), UK MHRA, ANVISA (Brazil), NPRA (Malaysia), GCC-DR, TITCK (Turkey), WHO, MoH Oman, MCC (South Africa),CAP, NABL, and others.Additional information:Job offer: On successful conversion to a permanent employee, the candidate can expect a salary of ₹ 225000 to 450000/year

Responsibilities

Note: These statements reflect the general description of the position and are not intended to be an all-inclusive list of tasks to which employee may be assigned

Selected intern's day-to-day responsibilities include:

1. Develop, validate and review SAS codes and outputs which transform raw data to CDISC, SDTM & ADaM standards.

2. Prepare and review documents related to study and CDISC package.

3. Review and provide necessary input in database design template and eCRF.

4. Identify data quality issues and communicate to respective stakeholders.

5. Maintain all necessary records for the reporting phase of the study.

6. Perform the validation of the software/programs used for analysis of statistical data.

7. Write and revise SOPs as per need and maintain awareness of and adherence to all current SOPs.

8. Conforms to training schedule for own position and maintains awareness of SOP content, according to company requirements.