
Senior Clinical Data Analyst
2 weeks ago
Seeking a skilled Clinical SAS Programmer to join our team. Below are the key responsibilities and requirements.
Key ResponsibilitiesAs a Clinical SAS Programmer, you will be responsible for:
- Designing and developing clinical trial data management systems using SAS EG/Studio.
- Creating and maintaining datasets, macros, and programs to support clinical trials.
- Collaborating with cross-functional teams to ensure data quality and compliance.
To succeed in this role, you will need:
- At least 5 years of experience in clinical domain, with relevant skills in SDTM, ADAM, and TLF.
- Proven track record of working on ADAM and TFL deliverables in multiple therapeutic areas and phases.
- Experience creating and working with utility macros.
- Strong analytical and problem-solving skills, with excellent communication and interpersonal skills.
- Proficiency in Unix environment and programming languages such as SAS.
- Prior experience in vaccines or oncology is an added advantage.
As a member of our team, you can expect:
- A dynamic and collaborative work environment.
- Opportunities for professional growth and development.
- Competitive compensation and benefits package.
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