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AbbVie
The Clinical Research Associate II is responsible for ensuring the successful conduct of clinical trials in oncology, focusing on data integrity and compliance.
F.F
FTINC Fortrea
The TMF Lead II manages the Trial Master File for clinical trials, ensuring compliance and readiness for inspections.
AbbVie
The Clinical Research Associate II is responsible for overseeing clinical trials and ensuring compliance with regulatory standards while enhancing site engagement.
AbbVie
AbbVie is seeking a Senior Manager to lead initiatives for improving diversity and inclusion in clinical trials.
AbbVie
The Clinical Research Associate II plays a key role in advancing clinical trials by ensuring effective site engagement and compliance.
ClinChoice
Seeking a Principal Statistical Programmer Consultant to lead programming efforts for clinical studies in Oncology.
D.T
Dyne Therapeutics
The Associate Director, Medical Writing is responsible for preparing high-quality clinical and regulatory documents for Dyne Therapeutics.
AbbVie
The Associate Director, Global Site Management oversees the strategic direction and execution of clinical site management within a therapeutic area.
P.P.M
Praxis Precision Medicines
Join Praxis as a Clinical Trial Manager to oversee impactful clinical studies and ensure high-quality trial management.
Alimentiv
The Clinical Operations Lead oversees clinical project operations, ensuring compliance and effective management of CRAs.
Alimentiv
The Senior Clinical Operations Lead manages clinical operations for projects, ensuring compliance and effective oversight of CRAs and investigator sites.
F.F.P
FTPHP Fortrea Philippines
The TMF Classifier I manages document classification and ensures compliance within clinical studies.
BlueRock Therapeutics
The Director of Clinical Operations Quality leads the development of SOPs and ensures compliance in clinical studies at BlueRock Therapeutics.
W.C
WEP Clinical
Join WEP Clinical as an Associate Director, Clinical Monitoring to lead teams in advancing clinical trials and innovative therapies.
Prokidney
The Manager, Regulatory CMC will oversee regulatory activities related to the development and commercialization of biotechnology products.