11 Remote Jobs at MMS

MMS is seeking a Senior Manager for Clinical Trial Transparency & Disclosure to lead a team and manage client interactions in a remote setting.

The Senior Medical Writer will write and edit clinical documents while ensuring compliance with regulatory standards.

Join MMS as an Experienced Biostatistics Consultant and contribute to innovative clinical research projects in a remote setting.

Join MMS as a Senior Medical Writing Consultant to produce high-quality clinical documents for the pharmaceutical industry.

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.

The Senior Medical Writer will create and edit clinical development documents for the pharmaceutical industry.

The Project Manager II position at MMS involves managing biometric deliverables and ensuring project success in the life sciences sector.

MMS is seeking a Principal Medical Writer to produce and manage regulatory documents for clinical trials.

The Senior Quality and Compliance Specialist ensures regulatory compliance and conducts GCP audits for MMS.

The Principal Medical Writer will be responsible for writing and editing clinical development documents and managing regulatory submissions.

The Senior Medical Writer will be responsible for writing and editing clinical documents while working remotely from South Africa.