Join a forward-thinking environment where your expertise in statistics will drive impactful projects within the pharmaceutical industry. This position promises to be an exciting opportunity for professionals eager to contribute to significant advancements in biologics.
As an ideal candidate, you are a proficient
CMC Statistician
with a robust background in statistical methodologies and programming. If you are passionate about statistical analysis and thrive in a collaborative setting, this role is designed for you.
* You handle internal statistical requests
* You perform Design of Experiments (DoE) to aid in decision-making.
* You conduct statistical analyses for both development and quality control, particularly regarding bioassays.
* You utilize statistical programming primarily in
R
and some
SAS
for transitions.
* You write comprehensive reports in
English
.
* You collaborate effectively with internal clients and cross-functional teams.
What are we looking for?
* You have a
Master's degree in Statistics
.
* You possess strong statistical skills, including experience with mixed models.
* You are proficient in
R programming
(mandatory).
* You have knowledge of Design of Experiments (DoE).
* You are an effective communicator, particularly in
English
(fluent in both written and spoken).
* You may have experience in pharma or CMC.
* You possess knowledge of bioassays and USP guidelines (1032, 1033, 1034).
* You are familiar with stability studies as per ICH guidelines.
* A
PhD
is preferred but not required.
* You have
French
language skills, which aid in integration.
* You might have basic knowledge of
SAS
for transitioning purposes.