Are you looking for a rewarding career in the clinical research and healthcare industry? Parexel, a leading global biopharmaceutical services organization, is hiring for two key positions: Statistical Programmer II in Mumbai and Clinical Operations Assistant in Bengaluru. If you’re passionate about improving global health and want to contribute to life-changing therapies, this is your chance to join a world-class team.
1. Statistical Programmer II – Mumbai ( 2 – 5 Years)
Job ID: R0000029231
Location: Mumbai, India
Job Type: Full-time
Application Deadline: March 2, 2025 (5 days left to apply)
About the Role
As a Statistical Programmer II at Parexel, you’ll play a crucial role in supporting clinical trials and ensuring the accuracy and efficiency of data analysis. Your work will directly contribute to the development of therapies that benefit patients worldwide.
Key Responsibilities
- Assist in project start-up activities, including creating global programs and tracking documentation.
- Perform statistical programming to produce derived datasets (e.g., SDTM, ADaM), tables, figures, and data listings.
- Ensure compliance with SOPs, ICH-GCP, and regulatory standards like CDISC and 21 CFR Part 11.
- Provide training and mentorship to team members.
- Participate in process improvement initiatives to enhance quality and efficiency.
Skills and Qualifications
- Proficiency in SAS programming.
- Strong analytical skills and attention to detail.
- Knowledge of clinical trial processes and regulatory requirements.
- Ability to manage competing priorities in a fast-paced environment.
- Excellent communication skills in English.
Education and Experience
- Degree in a relevant discipline (e.g., Statistics, Computer Science, Life Sciences) or equivalent work experience.
- Experience in clinical research or pharmaceutical industry preferred.
2. Clinical Operations Assistant – Bengaluru ( 0 – 1 Year)
Job ID: R0000027228
Location: Bengaluru, India
Job Type: Full-time
About the Role
The Clinical Operations Assistant (COA) role is ideal for individuals who are detail-oriented and passionate about supporting clinical trials. You’ll be responsible for maintaining central files, ensuring compliance, and assisting site management teams.
Key Responsibilities
- Track, scan, and file study documents in accordance with the Central File Maintenance Plan (CFMP).
- Support site management teams with administrative tasks and document QC.
- Manage clinical trial management systems (CTMS) and study-specific trackers.
- Organize translations of study documents and process payments/invoices.
- Ensure compliance with regulatory requirements and internal SOPs.
Skills and Qualifications
- Fluency in Japanese (N2, N3 level) for reading, writing, and speaking.
- Strong problem-solving and organizational skills.
- Experience in CROs or the life sciences industry is a plus.
- Excellent interpersonal and communication skills.
Education and Experience
- Degree in biological sciences, pharmacy, or a related field (or equivalent experience).
- Understanding of clinical trial methodology and terminology.
Why Join Parexel?
At Parexel, we’re driven by a shared mission to improve global health. Here’s why you should consider joining our team:
- Impactful Work: Contribute to the development of therapies that benefit patients worldwide.
- Global Opportunities: Work with a diverse, international team.
- Professional Growth: Access to training and mentorship programs.
- Innovative Environment: Be part of a company that values quality, innovation, and collaboration.
Application Link For Statistical Programmer II
Application Link For Clinical Operations Assistant
