Medical Affairs-Assistant Manager/Deputy Manager
Hetero
Date: 3 weeks ago
City: Hyderabad, Telangana
Contract type: Full time
Job Description:
Position Overview:
We are looking for a skilled and detail-oriented Clinical SAS Programmer to join our team in a clinical research environment. The ideal candidate will have experience developing and validating SAS programs for clinical trials and a strong understanding of statistical analysis. This role requires expertise in SAS programming, particularly with advanced features and SAS Macro language, along with excellent communication skills.
Key Responsibilities:
Position Overview:
We are looking for a skilled and detail-oriented Clinical SAS Programmer to join our team in a clinical research environment. The ideal candidate will have experience developing and validating SAS programs for clinical trials and a strong understanding of statistical analysis. This role requires expertise in SAS programming, particularly with advanced features and SAS Macro language, along with excellent communication skills.
Key Responsibilities:
- Develop, test, and validate SAS programs to support clinical research and analysis in clinical trials.
- Use statistical analysis skills to generate datasets, tables, listings, and figures for clinical study reports.
- Ensure SAS programs and outputs meet regulatory and client requirements.
- Utilize SAS Macro language and other advanced programming techniques to improve coding efficiency and data analysis.
- Work closely with clinical research teams to provide programming support, including data validation and reporting.
- Document and maintain all programming work in a clear and organized way to ensure reproducibility.
- Identify and solve any programming issues or discrepancies in datasets and analysis outputs.
- Stay updated on regulatory guidelines and standards such as FDA, EMEA, and ICH GCP in clinical trials.
- Proven experience as a Clinical SAS Programmer, preferably in a pharmaceutical or clinical research organization.
- Strong background in developing and validating SAS programs for clinical research.
- Good understanding of statistical analysis and its application in clinical trials.
- Proficiency in using SAS Macro language and other advanced SAS programming techniques.
- Strong attention to detail and problem-solving skills.
- Excellent communication skills, both written and verbal, to collaborate with teams and present results.
- Ability to work independently and manage multiple tasks in a fast-paced environment.
- Bachelor's or Master's degree in Computer Science, Statistics, Life Sciences, or a related field.
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