Dear Student,
Greetings!!
It gives us immense pleasure to announce that Axis Clinicals has shown interest in hiring talent from Clinilaunch Research Institute.
Company Details:
Axis Clinicals, a renowned name in the clinical research and bioanalytical industry, is offering an exciting opportunity for freshers (male) to join as Trainee Research Associates – Bioanalytical in Hyderabad. This role is ideal for candidates with a background in biological sciences, pharmacy, or clinical research who are looking to kickstart their careers in a dynamic and growing field. With a competitive salary range of INR 50,000 to 2 Lakhs per annum, this position is a great stepping stone for aspiring professionals.
Website: https://axisclinicals.com/
Job Type: Private
Hiring For: Axis Clinicals
Job Role: SAS Programmer
Industry: Bioanalytical Industry
Job Priority: Normal
Job Nature: Office
Job Mode: Full Time
Job Position: Permanent
Job Location: Hyderabad
Salary: 2.5LPA
Experience Range: 0-4 Years (Fresher Only)
Qualification: Msc in Statistics or Biostatistics & SAS Certified only
Bond: 2-year bond with the requirement to submit the original 10th-grade mark sheet during the bond period.
Job Summary:
We are seeking a motivated and detail-oriented fresh graduate to join our team as a Trainee Clinical SAS Programmer. In this role, you will be responsible for assisting in the development, validation, and analysis of clinical data using SAS software in clinical trials. You will work closely with senior programmers and other cross-functional teams to ensure the accuracy and integrity of clinical trial data while adhering to regulatory guidelines.
Key Responsibilities:
* Assist in the development, testing, and maintenance of SAS programs to manage clinical trial data, including datasets, tables, listings, and figures.
* Support the creation and validation of standard clinical trial datasets, including SDTM, ADaM, and other regulatory-compliant formats.
* Participate in the analysis and reporting of clinical trial data in accordance with the project specifications.
* Collaborate with the clinical data management, biostatistics, and other departments to ensure seamless data flow and integrity.
* Perform data review and quality checks to ensure accurate data submission.
* Assist in generating datasets, reports, and analysis outputs for submission to regulatory authorities (e.g., FDA, EMA).
* Follow Good Clinical Practice (GCP), 21 CFR Part 11, and other regulatory standards in programming activities.
* Work with the senior team members to troubleshoot and resolve any programming issues or data discrepancies.
* Participate in regular project meetings and contribute to status updates.
* Document programming activities and outputs according to internal procedures and quality standards.
Requirements:
* Basic knowledge of SAS programming language is a plus.
* Familiarity with clinical trial processes and terminology is an advantage.
* Strong analytical and problem-solving skills.
* Attention to detail and ability to handle multiple tasks simultaneously.
* Good communication and interpersonal skills to work in a collaborative team environment.
* A keen interest in clinical data analysis and programming.
* Ability to learn quickly and adapt to new tools and technologies.
* Preferred Skills (optional but advantageous):
* Internship or project experience related to clinical data or SAS programming.
* Exposure to clinical trial management systems or related software.
* Knowledge of clinical data standards (e.g., CDISC, SDTM, ADaM).
Date Published: 25-03-2025
Through: Valid: 26-03-2025 Before 11AM
Note : CLRI Resume is Mandatory
Application Link : https://forms.gle/WJdoaWjb6TYe6KNy8
In Case of any Queries Contact Harshitha - 8050234854
Regards,
Harshitha
Placement Team