Title: Manager 1, Statistical Programming Business Unit: Global Clinical Development Job Grade: G10 Location: Remote/Hybrid At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment …
Skills: SAS Programming, CDISC Standards, SDTM, ADaM, Clinical Trial Data Processing
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Full-time
bachelor degree
Posted 34d ago
Apply by Jul 31
~40 hrs/week
Responsibilities
Lead and support all statistical programming activities to ensure high-quality deliverables for clinical studies and regulatory submissions. This includes developing SDTM/ADaM datasets, maintaining programming standards, and mentoring junior programmers.
Requirements
Requires a minimum of a Bachelor's degree in a quantitative or life science field and 8+ years of clinical trial programming experience. Proficiency in SAS is essential, with strong knowledge of CDISC standards and regulatory guidelines.
Full job description
Title: Manager 1, Statistical Programming
Business Unit: Global Clinical Development
Job Grade: G10
Location: Remote/Hybrid
At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
JOB DESCRIPTION:
The Manager 1 will provide comprehensive programming expertise to lead and support all programming activities as per the project strategies. The incumbent should be able to work independently implementing and executing the programming and project standards to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal partnering functions, stakeholders, and external functional service providers to ensure all the programming deliverables are delivered in timely manner with high quality. The incumbent will participate in and contribute to department goals, SOPs, macros, SME topics and act as a technical expertise to provide guidelines on complex programming tasks and standards.
In this role, a typical day might include the following:
Lead statistical programming activities for a therapeutic area or compound/indication within multiple studies/projects in various study activities to ensure timely and high-quality programming deliverables in assigned projects and areas.
Develop and maintain programming documentations following programming standards and processes. Create CDISC standard SDTM mapping specifications and ADaM specifications.
• Develop and oversee the development of SAS programs for the creation of SDTM and ADaM datasets following CDISC standards and reports (Tables, Listings and Figures).
Contribute to the development of standard macros, participate in establishing and maintaining statistical programming standards.
Participate in the CRF annotation, review of SAP, TLFs specifications development and TLFs review.
Handle all P21 related items and eCRT package including aCRF, define.XML, cSDRG, ADRG and ARM for the regulatory submission to FDA/EMA/PMDA or other agencies.
Support global regulatory authority submissions following the guidelines (sdTCG, DSC, eCTD etc.) and working closely with partnering functions to address health authority requests.
Demonstrate company values by demonstrating excellence, competence, collaboration, innovation, respect, ownership, team work and accountability.
Understand the scope of work, plan and complete the deliveries and timelines with the study team, programming lead and management.
Participate and contribute towards department goals, SOPs, training guidelines and SME topics.
Mentor and Coach new hires and junior programmers.
This Role May Be For You If Have
Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. Working knowledge of other programming languages such as R, Python etc. is a plus.
Great knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles) and regulatory submissions (NDA, ANDA etc.).
Great working knowledge of implementing CDISC standards, Regulatory guidance and TAUG.
Ability to work independently and on global interdisciplinary teams. Good organizational, interpersonal, and communication skills. Positive attitude, team player and growth mindset.
Problem solving and innovative skills that demonstrate initiative and motivation.
Hands-on programming as well as people and process management experience.
Demonstrated and applied SAS programming skills. SAS certificates a plus.
Educational Qualification: Minimum Bachelor’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.
Experience: 8+ years of programming experience in processing clinical trial data in the biotechnology, pharmaceutical, CRO or health care related industry.
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!
Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
Sun Pharma is the world's fourth-largest speciality generic pharmaceutical company and No. 1 in India. We provide high-quality, affordable medicines trusted by customers and patients in over 100 countries. Sun Pharma's global presence is supported by more than 40 manufacturing facilities spread across 5 continents, R&D centres across the globe, and a multicultural workforce comprising over 50 nationalities. Sun Pharma fosters excellence through innovation supported by strong R&D capabilities comprising around 3,000 scientists and R&D investments of over 6-8% of annual revenues.
At Sun, our people are our greatest asset. Ours has never been a story of individual brilliance but of cultivating a culture of realising collective potential. In our journey, everyone is enabled to take charge in an environment that offers limitless growth opportunities. We are with you every step of the way, so you can shine for years to come.
With the launch of our Employee Value Proposition (EVP), we define our promise to ‘Create Your Own Sunshine'—driven by the three pillars of Better Every Day, Take Charge, and Thrive Together. These pillars drive progress at Sun so that people can achieve what they would have thought impossible. Learn more about our EVP here: https://sunpharma.com/careers/
Offices: Sun House, CTS No. 201 B/1,, Western Express Highway, Goregaon East, Mumbai, Maharastra 400063, IN
How many Science & Research jobs are open in Gurgaon, India right now?
There are currently 151 open science & research positions in Gurgaon, India listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Gurgaon, India?
Companies currently hiring include SUN PHARMA, 1Lattice, American Express, Sage, Gartner, among others. Browse the listings above to see every active employer.
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