Dear Student,
Greetings!
It gives us immense pleasure to announce that Croissance Clinical research has shown interest in hiring talent from Clinilaunch Research Institute.
About – Croissance Clinical research
About company:
Croissance Clinical research is a full-fledged CRO providing services for Pharmaceutical, bio- technology and medical devices companies.
Croissance Clinical Research applies innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments.
Our experienced project managers and the team leaders will ensure, that all the services are conducted in accordance with the study protocol, ICH-GCP guidelines and applicable regulatory requirements.
Company: Croissance Clinical research
Website: http://www.croissancecr.com
Job Type: Private
Job Role: CDM, Trainee Clinical SAS
Industry: Biotechnology Research
Job Priority: Normal
Job Nature: Work from Office
Job Mode: Full Time, Work from Office.
Job Position: Permanent
Job Location: Hyderabad, Telangana
Job Type: Full-Time
Qualification: B,Sc Bio technology, M,Sc Bio technology, B,Sc Statistics, M,Sc Statistics, B Tech Biotechnology- for SAS, All life Science for CDM
Date Published: 24-3-2025
Valid Through: 24-3-2025 (06:00 PM)
Interview mode: Walk in
Experience: Only Freshers
Salary: As per industrial norms
JD for Trainee Clinical SAS
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:
Bachelor’s degree in Life Sciences, Computer Science, Statistics, Mathematics, or related field.
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).
JD for Clinical Data Management
Job Summary:
Key Responsibilities:
Data Management Support: Assist in the setup, maintenance, and troubleshooting of clinical trial databases, ensuring the accuracy and consistency of data collected throughout the trial.
Data Review & Validation: Help validate incoming data for completeness and consistency, and assist in identifying and resolving discrepancies.
Case Report Form (CRF) Management: Support the creation, management, and revision of Case Report Forms (CRFs) to ensure they meet study requirements.
Electronic Data Capture (EDC): Assist in the implementation and monitoring of EDC systems, ensuring proper data entry and resolving any issues related to the system.
Query Management: Assist in generating and managing data queries for clinical trial sites, ensuring timely resolution and follow-up.
Study Documentation: Help maintain accurate records of data management activities, ensuring compliance with regulatory requirements and internal guidelines.
Collaboration: Work with cross-functional teams including clinical operations, biostatistics, and regulatory affairs to ensure timely and accurate data collection, review, and reporting.
Compliance with Regulations: Ensure data management processes comply with industry regulations such as Good Clinical Practice (GCP), 21 CFR Part 11, and ICH guidelines.
Reporting & Tracking: Assist in preparing reports and tracking progress to ensure data management milestones are met according to timelines.
Requirements:
Skills:
Strong attention to detail and accuracy.
Good organizational skills with the ability to manage multiple tasks.
Ability to work collaboratively within a team.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Attributes:
Strong communication skills, both written and verbal.
Eagerness to learn and develop in the clinical research field.
Ability to adapt to new software and technologies.
Preferred (but not required):
Familiarity with clinical trial processes and data management terminology.
Experience with Electronic Data Capture (EDC) systems or clinical data management software is a plus.
Application Link: https://forms.gle/9Zp9geKxbqXPdUGD7
In Case of any Queries Contact Priyanka C - 8904527576/ Mugesh raj – 8951764077
Regards,
Placement Team