Clinical Research Trainer

3 days ago

Bengaluru, India Airvin Skills Training and Consulting Pvt Ltd Full time

**Responsibilities**:

- Collaborate with cross-functional teams, including biostatisticians, data managers, and clinical research associates, to develop programming specifications and data analysis plans.
- Design and develop SAS programs to generate tables, listings, and graphs (TLGs) for clinical study reports, regulatory submissions, and other study-related documents.
- Perform data validation and quality control checks to ensure accuracy and integrity of clinical trial data.
- Create and maintain SAS datasets, including data transformation, cleaning, and integration from multiple sources.
- Develop and validate SAS macros and utilities to automate repetitive tasks and improve programming efficiency.
- Ensure compliance with regulatory guidelines, industry standards, and company SOPs in programming and data handling.
- Collaborate with statisticians to provide input on statistical analysis plans and assist with statistical programming tasks as needed.
- Conduct ad-hoc data analyses and generate reports in response to internal and external requests.
- Participate in data review meetings and provide support for data-related queries from internal and external stakeholders.
- Stay updated on emerging trends, new methodologies, and advancements in SAS programming techniques.
- Document programming processes, datasets, and programming specifications in accordance with company standards.
- Contribute to process improvement initiatives and share best practices within the programming team.

Qualifications and Skills:

- Bachelor's or Master's degree in a relevant scientific discipline (e.g., statistics, biostatistics, computer science).
- Minimum of 3 years of experience as a Clinical SAS Programmer in the pharmaceutical, biotech, or clinical research industry.
- Proficiency in SAS programming, including SAS/Base, SAS/STAT, SAS/Graph, and SAS/Macro.
- Strong understanding of clinical trial data structures, CDISC standards (SDTM and ADaM), and regulatory guidelines (e.g., ICH-GCP).
- Experience in generating TLGs, tables, and figures for clinical study reports and regulatory submissions.
- Solid knowledge of data management principles and processes.
- Familiarity with data visualization tools and techniques.
- Excellent problem-solving and analytical skills.
- Detail-oriented with the ability to work on multiple projects and meet deadlines.
- Good communication and interpersonal skills to collaborate effectively with cross-functional teams.
- Knowledge of programming languages such as Python or R is a plus.
- Certification in SAS programming or clinical data management is desirable.

Salary and Benefits:

- Competitive salary based on qualifications and experience.
- Professional development opportunities to enhance SAS programming skills and knowledge.

**Job Types**: Full-time, Fresher

**Salary**: From ₹25,000.00 per month

**Benefits**:

- Cell phone reimbursement

Schedule:

- Day shift
- Morning shift

Supplemental pay types:

- Commission pay
- Performance bonus

Ability to commute/relocate:

- Bangalore, Karnataka: Reliably commute or planning to relocate before starting work (required)

**Speak with the employer**
+91 +91 79966 99942

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