Parexel
The Clinical Trial Submission Lead at Parexel oversees the end-to-end planning, coordination, and execution of Clinical Trial Applications across EU and global regions. This role ensures timely, compliant submissions through cross-functional collaboration, proactive risk management, and deep regulatory expertise in a matrixed environment.
Headquarters
Raleigh, North Carolina, United States
Company Size
10001+ employees
Founded
1982
For over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Parexel.
Parexel didn’t post a salary, so this is our estimate from similar listings.
29% below the average for this role
Update: How 7 companies delivered on NC job promises
1 month ago
Regulatory Submission Professional - Clinical Trial Submissions in EU
Novo Nordisk A/S
Regulatory Submission Professional - Clinical Trial Submissions in EU
Novo Nordisk A/S
Reg Submission Specialist, SDE - Investigational
GSK plc
Senior Regulatory Affairs Specialist
Indero
Regulatory Affairs Specialist-Poland
Indero
EU CTR Submission Lead
biogen