Openings in Accenture for Regulatory affairs department

Experience : 1.5 to 5 years with regulatory markets (US and Europe)

Roles and responsibility :

Candidates are responsible for CMC/labelling documents

need to have knowledge on Module 4 pre clinical reports and Module 3 technical CMC documents

Conduct review of complete IND, CTA application eCTD xml backbones for eCTD compliance and accuracy.

Need to have good communication skills and adhere to the standards of Accenture operating procedures.

Able to work in minimal supervision

Interested candidates can send resumes to [email protected] with Subject line as RA.

Openings in Accenture for Regulatory affairs department - Send resumes