Home
Communities
Companies
- Companies
  
  Discover best places to work
- Compare Companies
  
  Compare & find best workplace
- Add Office Photos
  
  Bring your workplace to life
- Add Company Benefits
  
  Highlight your company's perks
Reviews
- Company reviews
  
  Read reviews for 6L+ companies
- Write a review
  
  Rate your former or current company
Salaries
- Browse salaries
  
  Discover salaries for 6L+ companies
- Salary calculator
  
  Calculate your take home salary
- Are you paid fairly?
  
  Check your market value
- Share your salary
  
  Help other jobseekers
Interviews
- Company interviews
  
  Read interviews for 40K+ companies
- Campus placements
  
  Interviews questions for 1K+ colleges
- Share interview questions
  
  Contribute your interview questions
Jobs
Awards

WINNERS AWAITED!
- ABECA 2025
  
  WINNERS AWAITED!
  
  AmbitionBox Employee Choice Awards - 4th Edition
- ABECA 2024
  
  AmbitionBox Employee Choice Awards - 3rd Edition
- AmbitionBox Best Places to Work 2022
  
  2nd Edition
- AmbitionBox Best Places to Work 2021
  
  1st Edition

For Employers

Add office photos

Employer? Claim Account for FREE

Sanofi

Compare

4.3

based on 1.1k Reviews

Proud winner of ABECA 2024 - AmbitionBox Employee Choice Awards

Top Rated Mid-Sized Company - 2024

Top Rated Company for Women - 2024

Top Rated Pharma Company - 2024

161 Sanofi Jobs

Early Phase Programming Team Lead

Sanofi India Ltd

4.3

based on 1.1k Reviews

2-6 years

Hyderabad / Secunderabad

1 vacancy

Early Phase Programming Team Lead

Sanofi

posted 4mon ago

Job Role Insights

Flexible timing

Key skills for the job

Outsourcing Healthcare Project Management Clinical SAS Programming Statistical Programming Process Optimization

+ 1 more

Job Description

As an Early Phase Programming Team Lead you will Lead one or more statistical programming project team(s)
Responsible for all programming activities at the project/indication level
Contribute to department initiatives and task forces
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people s lives
we're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible

Major Responsibilities:

Programming Project Lead (PPL) of a moderate size project / one or several indications of a project in late phase clinical development or multiple projects in early or post-marketing phase. With limited direction from group manager, plan and execute statistical programming activities for responsible project(s).
Provide leadership, guidance, and hands-on support to ensure high quality and timely statistical programming deliverables within a project, ensure technical validity, compliance to internal standards and SOPs, regulatory requirements.
Plan and track programming project activities, timelines, and resource use in cross-site global setting; provide justification for planned resource needs, seek to optimize resource utilization thru efficient and we'll-managed resource allocation and across projects or areas.
Ensure standardization and consistency in specifications and programming deliverables across individual studies and for integrated analyses . Provide technical guidance and leadership to metadata specifications and project/study specific data requirements.
Lead regulatory submission activities, including electronic submission packages. Supervise the quality controls (QC) methods and processes for programming deliverables in both study and submission level activities.
Provide guidance to junior staff on programming techniques, project management and implementation of standards. Collaborate effectively with project statistician and with other functions in the aligned project team; participate in clinical project meetings and provide inputs, whenever relevant
Lead oversight activities for outsourcing engagements; guide team members to effectively interact with external resources. Participate in departmental initiatives; provide inputs to programming standardization and process optimization.

About you

Experience: P rogramming experience preferably in processing clinical trial data in the pharmaceutical industry .
Soft skills: Collaborative and progressive mindset and a potential for future, Agility to quickly acquire new skills.
Thorough understanding of pharmaceutical clinical development (ie, statistical concepts, techniques, and clinical trial principles) and ability to lead regulatory submissions.
Technical skills: Excellent technical skills in statistical programming, with advanced knowledge in SAS and Knowledge about R Programming would be an advantage.
Education: Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field.
Languages: Highly effective communication in English, both oral and written.

Why choose us

Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, we'll-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and we'llbeing benefits including high-quality healthcare, prevention and we'llness programs and at least 14 weeks gender-neutral parental leave.
Build, develop and manage a statistics team support multiple TAs and different clinical phases
Develop a career of being an influential statistician
Gain international clinical trial experiences and communicate with Health Authorities worldwide