Join Medpace in Navi Mumbai: Shape the Future of Clinical Research!
Summary: Medpace, a leading global Clinical Research Organization (CRO), is seeking talented and motivated individuals to join our growing biometrics team in Navi Mumbai. We have openings for both a SAS Programmer and a Clinical Database Designer. These roles offer a fantastic opportunity to contribute to cutting-edge clinical trials, develop your skills in a supportive environment, and build a rewarding career in the dynamic field of clinical research. If you’re passionate about data, precision, and making a difference in healthcare, we encourage you to apply!
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We embrace innovation, foster collaboration, and are committed to delivering exceptional results for our clients.
We are currently seeking qualified candidates for the following positions in our Navi Mumbai office:
1. SAS Programmer – Navi Mumbai
Are you a skilled SAS programmer looking to apply your expertise in the critical field of clinical research? As a SAS Programmer at Medpace, you will play a vital role in ensuring the integrity and accuracy of clinical data, contributing directly to the success of our clinical trials.
Key Responsibilities:
- Develop, test, and validate SAS programs to generate analysis datasets, tables, listings, and figures (TLFs) according to study specifications and regulatory requirements.
- Maintain and manage mapped clinical databases using SAS programming techniques.
- Design and implement data edit checks using SAS to ensure data quality and consistency for external data sources.
- Collaborate closely with Data Management teams to facilitate data transfers, clarify data specifications, and resolve data-related issues.
- Contribute to the development and maintenance of SAS programming standards and best practices.
- Participate in the review and validation of statistical analysis plans (SAPs).
- Ensure adherence to Good Clinical Programming (GCP) guidelines and Standard Operating Procedures (SOPs).
Qualifications:
- Bachelor’s or Master’s degree in Statistics, Mathematics, Health Informatics, Data Science, Computer Science, Life Sciences, or a related field.
- SAS certification is highly preferred.
- 1–2 years of practical experience in SAS programming, preferably within the pharmaceutical or clinical research industry.
- A solid understanding of data management principles and database structures.
- Proficiency in using SAS Base, SAS Macro Language, and SAS procedures for data manipulation, analysis, and reporting.
- Excellent written and verbal communication skills, with the ability to effectively communicate technical concepts to both technical and non-technical audiences.
- Strong analytical and problem-solving skills, with meticulous attention to detail.
- Ability to work independently and as part of a team, effectively managing multiple tasks and priorities.
2. Clinical Database Designer – Navi Mumbai
Are you detail-oriented and passionate about ensuring the quality and integrity of clinical trial data? Join Medpace as a Clinical Database Designer and contribute to the development and maintenance of robust and compliant electronic Case Report Forms (eCRFs) for our clinical studies.
Key Responsibilities:
- Design, develop, and maintain eCRF specifications and edit check specifications in accordance with CDISC (Clinical Data Interchange Standards Consortium) standards and study protocols.
- Customize library eCRFs to meet specific study requirements and manage specifications throughout the database build and database lock process.
- Perform thorough User Acceptance Testing (UAT) and validation of eCRFs and edit checks to ensure accuracy, functionality, and compliance.
- Liaise effectively with Data Managers, Sponsors, and Clinical Database Programmers to ensure seamless communication and collaboration.
- Lead eCRF review meetings, providing guidance and ensuring alignment with study objectives.
- Prepare EDC (Electronic Data Capture) system reports using Business Objects and JReview to monitor data quality and identify potential issues.
- Contribute to the development and maintenance of database design standards and best practices.
- Ensure compliance with relevant regulatory guidelines, including 21 CFR Part 11.
Qualifications:
- Bachelor’s or Master’s degree in Life Sciences or Computer Science.
- Minimum 1 year of experience in EDC UAT or specification development, preferably within the pharmaceutical or clinical research industry.
- Familiarity with CDISC standards, including CDASH (Clinical Data Acquisition Standards Harmonization).
- Experience working with EDC systems such as Medidata Rave, Oracle Clinical, or similar platforms.
- Excellent attention to detail and organizational skills, with the ability to manage multiple tasks and priorities effectively.
- Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse teams.
- A proactive and solution-oriented approach to problem-solving.
Why Choose Medpace?
At Medpace, we are committed to providing our employees with a rewarding and supportive work environment where they can thrive and make a meaningful impact. We offer:
- Flexible work environment.
- Competitive salary and benefits package.
- Structured career growth opportunities with defined learning paths.
- Comprehensive employee wellness programs.
- Global exposure to top-tier clinical trials across a variety of therapeutic areas.
- Recognition as a leading CRO by Forbes and CRO Leadership Awards.
We believe that our employees are our greatest asset, and we are dedicated to fostering a culture of innovation, collaboration, and excellence. Join us and be a part of a team that is shaping the future of clinical research!
How to Apply:
Interested and qualified candidates are encouraged to apply online.