Service/Supplier jobs in Maryland
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Primary responsibilities include managing team of 5-7 Clinical Information Specialists...
This position will act as a Clinical Research Ethicist.
Perform various tasks in support of clinical research including adverse event analysis and processing...
This position will manage and process SAEs; assist in the preparation of reports; generate specified data reports from...
Preparing scientific and regulatory documents.
Prepare standard documentation supporting regulatory filings and distribution to stakeholders.
Responsible for verifying clinical compliance to applicable Standard Operating Procedures.
Preparing scientific and regulatory documents on behalf of government and private sector clients for submission to the FDA.
Assess GCP compliance risk areas and develop and implement risk mitigation measures.
Receipt and abstraction of protocol and/or contact information into the appropriate databases.