Job Summary
A clinical research company has a current position open for a Telecommute Principal Regulatory Submissions Medical Writer.
Candidates will be responsible for the following:
- Preparing clinical and regulatory documents as a Lead Writer or in a support function
- Acting as the point of contact between Medical Writing and both internal and external customers for specified projects
- Ensuring projects are completed according to contractual obligations and in a profitable manner
Applicants must meet the following qualifications:
- Ability to travel approximately 20% of the time
- Experience in regulatory submissions
- Ability to train and develop less experienced medical writers
