RemoteOtterRemoteOtterMMS
MMS is an award-winning, data-focused clinical research organization (CRO) that supports the pharmaceutical, biotech, and medical device industries. Recognized as a Great Place to Work certified organization, MMS boasts an exceptional culture and industry-leading employee retention rate. With a global presence across four continents, the company excels in providing scientific solutions to complex trial data and regulatory submission challenges. MMS is committed to fostering a collaborative and inclusive work environment, ensuring that employees can thrive while contributing to the future of clinical research.
MMS
MMS
The Senior Medical Writer will write and edit clinical documents while ensuring compliance with regulatory standards.
MMS
MMS
Join MMS as an Experienced Biostatistics Consultant and contribute to innovative clinical research projects in a remote setting.
MMS
MMS
Join MMS as a Senior Medical Writing Consultant to produce high-quality clinical documents for the pharmaceutical industry.
MMS
MMS
MMS is seeking a Director for their Regulatory and Medical Writing Team to lead and mentor a group of writers while managing client relationships and project risks.
MMS
MMS
The Senior Medical Writer will create and edit clinical development documents for the pharmaceutical industry.
MMS
MMS
The Project Manager II position at MMS involves managing biometric deliverables and ensuring project success in the life sciences sector.
MMS
MMS
MMS is seeking a Principal Medical Writer to produce and manage regulatory documents for clinical trials.
MMS
MMS
The Senior Quality and Compliance Specialist ensures regulatory compliance and conducts GCP audits for MMS.
MMS
MMS
The Principal Medical Writer will be responsible for writing and editing clinical development documents and managing regulatory submissions.
MMS
MMS
The Senior Medical Writer will be responsible for writing and editing clinical documents while working remotely from South Africa.
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