OrciMed Life Sciences Hiring Clinical Data Manager, Clinical SAS Programmer

- Exciting Career Opportunities for Life Sciences Professionals
- Why Join OrciMed Life Sciences?
- Open Positions at OrciMed Life Sciences
- Clinical Data Manager
- Clinical SAS Programmer
- Preferred Educational Background
- Location and Application Process
- Final Thoughts
- Summary Table
Clinical Research Jobs for Life Sciences Graduates | 3+ Years Experience Required
Explore Clinical Data Manager and SAS Programmer jobs at OrciMed Life Sciences. Openings for life sciences graduates with 3+ years’ experience. Location details inside.
Exciting Career Opportunities for Life Sciences Professionals
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📱 Join Click HereOrciMed Life Sciences, a rapidly growing leader in the healthcare analytics and clinical research domain, is currently expanding its clinical operations team. If you’re a skilled professional with a background in life sciences and a passion for clinical data, this could be the opportunity to elevate your career.
We are actively hiring for two key roles within our clinical research division: Clinical Data Manager and Clinical SAS Programmer. Candidates with a minimum of 3 years of industry experience and a strong foundation in clinical data management and programming are encouraged to apply.
Why Join OrciMed Life Sciences?
OrciMed offers an inclusive and dynamic work culture that prioritizes innovation, learning, and career growth. Our projects span global clinical trials, allowing our team to work with advanced tools and datasets that contribute to improved patient outcomes.
Open Positions at OrciMed Life Sciences
Clinical Data Manager
Responsibilities:
- Manage end-to-end CDM activities: Study Setup, Conduct, and Close-Out.
- Work on Medrio EDC systems for database build, validation, and data cleaning.
- Collaborate with cross-functional teams to ensure data quality and regulatory compliance.
Requirements:
- Minimum 3 years of hands-on experience in Clinical Data Management.
- Proficiency in Medrio EDC is mandatory.
- Excellent understanding of clinical trial protocols and GCP guidelines.
Clinical SAS Programmer
Responsibilities:
- Develop and validate datasets and TLFs (Tables, Listings, and Figures).
- Work on CDISC standards including SDTM and ADaM.
- Collaborate with biostatisticians and data managers to deliver accurate statistical outputs.
Requirements:
- 3+ years of experience in SAS programming in a clinical trial setting.
- Strong command over CDISC, SDTM, ADaM, and TLF creation.
- Familiarity with regulatory submission requirements.
Preferred Educational Background
Eligible candidates should have academic qualifications in one or more of the following disciplines:
Life Sciences, Biotechnology, Pharmacy, Clinical Research, Biomedical Sciences, Biostatistics, Data Science, or related fields.
These fields are foundational to understanding the nuances of clinical trials and statistical analysis in a regulated environment.
Location and Application Process
All roles are based at OrciMed Life Sciences’ designated clinical research hubs. Interested candidates are encouraged to apply promptly.
How to Apply:
Send your updated resume to: careers@orcimedlifesciences.com
Final Thoughts
These openings at OrciMed Life Sciences are ideal for candidates looking to build a long-term career in clinical research, SAS programming, or healthcare analytics. With industry-aligned exposure and high-growth potential, these roles offer both professional satisfaction and domain expertise.
Summary Table
Company Name | OrciMed Life Sciences |
---|---|
Current Vacancies | Clinical Data Manager, Clinical SAS Programmer |
Required Education | Life Sciences, Biotechnology, Pharmacy, Clinical Research, Biomedical Sciences |
Experience Required | Minimum 3 years in relevant field |
