This is an exciting opportunity to join our team as a Clinical Trials Lead Programmer.

As a key member of our programming team, you will be responsible for overseeing the statistical and programming aspects of multiple projects, acting as the lead programmer, project lead, or project oversight lead for a client/asset.

You will play a crucial role in the design, analysis, and reporting of clinical trials, ensuring adherence to regulatory requirements and industry standards.

Additionally, you will represent the department to clients, actively contributing to proposals and bids, and organizing teams to implement study strategies and ensure process and programming efficiencies.

This position may also involve managing a small team within the programming group.

Key Responsibilities:

1. Design, analyze, and report on clinical trials.
2. Ensure regulatory requirements and industry standards are met.
3. Represent the department to clients, contributing to proposals and bids.
4. Organize teams to implement study strategies and ensure process and programming efficiencies.
5. Manage a small team within the programming group (if applicable).

Requirements:

• MS/MA degree in computer science, statistics, biostatistics, mathematics or related field and at least 3 years of experience.
• Knowledge and background in statistics.
• Expert level knowledge and highly resourceful hands-on experiences in SDTMS/ADaMs/TLFs specifications and programming.
• Good Knowledge of Pinnacle 21.
• Strong SAS programming skills and understanding of database structures.
• Excellent written and verbal communication skills.

Why Join Us?

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.

Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects.

We are committed to diversity, inclusion, and equal opportunities.