About

At the forefront of the life sciences industry, TK-CHAIN embodies an amalgamation of innovation, service, and excellence. We're a holistic solution provider with a diverse portfolio spanning Clinical Research, Biostatistics, Regulatory Affairs, Computer System Validation (CSV), Gene Therapy, Data Science, and Personalized Medicine. Our core mission is to expedite healthcare advancements, revolutionize the life sciences landscape, and contribute towards enhancing and preserving human life. By creating a streamlined path from scientific research to commercial applications, we harness the power of technology and our unrivaled industry expertise. Understanding the unique needs of our clients, TK-CHAIN customizes solutions, delivering a variety of service models such as Full Service Provider (FSP), Staffing services, Global VMS Solutions, Managed Service Provider (MSP), Project-Based Service (PBS), Consulting Service (CS), and Contract Research Services (CRS). Operating across North America, and India, our global presence coupled with local insights equips us with a comprehensive understanding of diverse regulatory environments. At TK-CHAIN, we recognize the invaluable contributions of our team members and appreciate their role in our shared success and the significant influence we wield in the life sciences sector. Our dedicated professionals unite under a common objective - to leave a profound imprint on global healthcare. We invite you to join us in our transformative journey as we continue to fuel innovation, shape the life sciences industry's future, and contribute towards a healthier world for all. We are TK-CHAIN – innovating for a healthier future, today. 🔹Transforming Life Sciences | 🔹Saving Lives | 🔹Driving Innovation | 🔹Customized Solutions | 🔹Global Expertise

Jobs at TK-Chain

SAS Programmers

at TK-Chain

Posted by Aruna Sree

The recruiter has not been active on this job recently. You may apply but please expect a delayed response.

Chennai, Hyderabad

4 - 15 yrs

₹5L - ₹30L / yr

SAS

SAS/BASE

SAS/MACROS

SAS/GRAPH

SAS/STAT

+3 more

Job Overview: We are seeking a dedicated Senior Statistical Programmer to join our dynamic team. You will be responsible for the development, quality control, and documentation of statistical (SAS) programming deliverables for clinical research studies.

Key Responsibilities:

1. Lead and oversee the development of SAS programs for the management and statistical analysis of clinical trial data.

2. Develop, test, and validate statistical tables, listings, and graphs (TLGs) in support of the statistical analysis plan.

3. Support the generation and review of protocols, data management plans, study reports, and other regulatory documents.

4. Provide input to the statistical analysis plan, table shells, data integration plans, and mock-ups.

5. Ensure data quality by designing and validating key data checks and listings.

6. Develop specifications for derived datasets and perform data transformation as necessary.

7. Collaborate effectively with data management and biostatistics teams, clinicians, and other project stakeholders.

8. Guide junior programmers and provide mentoring as needed.

9. Keep abreast of new developments in SAS programming and clinical research, and act as a subject matter expert for the team.

Required Qualifications and Skills:

1. Bachelor's or master’s degree in Statistics, Mathematics, Computer Science, or a related field.

2. Minimum of 3 plus years of statistical programming experience in the pharmaceutical, biotech, or CRO industry.

3. Excellent SAS programming skills and proficiency in SAS/Base, SAS/Macro, SAS/Graph, and SAS/STAT.

4. Familiarity with CDISC SDTM and ADaM data standards.

5. In-depth understanding of clinical trial data and extremely complex statistical methods.

6. Excellent problem-solving skills and a proactive approach to identifying and resolving issues.

7. Strong written and verbal communication skills, with the ability to translate complex data into understandable results.

8. Proficiency in English, with excellent written and verbal communication skills.

9. Prior experience leading teams or projects is highly desirable.

Preferred Skills:

1. Experience in oncology, immunology, respiratory, infectious diseases, or neurosciences is a plus.

2. Knowledge of other statistical software such as R or Python is a plus.

3. Knowledge of regulatory guidelines (FDA/EMA/ICH) is preferred.