RemoteOtterRemoteOtterExplore 90 Remote Ich Guidelines Jobs
P.M
Parabilis Medicines
The Senior Director, Medical Writing will lead medical writing activities across clinical development at Parabilis Medicines, ensuring high-quality regulatory documentation.
Seqirus
Seqirus
The Associate Director Site Management & Oversight Lead oversees clinical trial site management to ensure compliance and operational efficiency.
CSL Plasma
The Lead Clinical Site Ambassador oversees clinical trials, ensuring compliance and operational efficiency while managing site relationships.
Precision Medicine Group
Seeking an experienced Senior Project Manager to lead clinical trials in Oncology within a global CRO environment.
Dianthus Therapeutics
The Associate Director, Medical Writing will lead the development of clinical and regulatory documents in a fully remote role.
PSI CRO
The Associate Medical Writer will be responsible for creating and reviewing clinical documentation in a remote setting.
Madrigal
Madrigal
Join Madrigal as a GMP Quality Assurance Specialist to ensure compliance with quality standards in a biopharmaceutical setting.
RayzeBio
RayzeBio
The Senior Manager, Clinical Program Management oversees clinical studies, ensuring compliance and timely delivery while managing teams and budgets.
G.S
Gilead Sciences
Join Gilead as a Clinical Trials Manager to oversee clinical studies and ensure compliance with regulatory standards.
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.