BioClin Pharma is a renowned company specializing in clinical research and pharmaceutical services. With a commitment to excellence and innovation, BioClin Pharma strives to provide high-quality solutions that meet the needs of clients in the healthcare industry. The company offers a dynamic and rewarding work environment, focusing on professional growth and skill development.
Job Responsibilities
As a SAS Programmer at BioClin Pharma, your key responsibilities will include:
- Developing and validating SAS programs for clinical trials and data analysis.
- Converting raw clinical trial data into analysis-ready datasets.
- Creating reports and summaries for regulatory submissions.
- Assisting in the design and implementation of statistical analysis plans.
- Collaborating with the clinical research team to ensure timely and accurate data reporting.
- Providing programming support for clinical trials and clinical data management.
Qualifications
To be considered for the SAS Programmer role, candidates should meet the following qualifications:
- A Bachelor’s degree in Computer Science, Life Sciences, or a related field.
- 0-2 years of experience in SAS programming, preferably in the clinical research or pharmaceutical industry.
- Knowledge of clinical trial data management and regulatory requirements.
Skills
The ideal candidate should possess the following skills:
- Proficiency in SAS programming for clinical trials and statistical analysis.
- Understanding of clinical trial data and regulatory reporting requirements.
- Strong problem-solving skills and attention to detail.
- Excellent communication and collaboration skills.
- Ability to work effectively in a fast-paced environment.
How to Apply
Interested candidates are invited to send their resume to hr@bioclinpharm.com. Please mention “SAS Programmer” in the subject line.
