This job has expired

Senior Associate Regulatory Affairs

Employer
i Pharm Consulting
Location
UK
Salary
Competitive
Closing date
27 Jul 2021

View more

Sector
Healthcare
Contract Type
Permanent
You need to sign in or create an account to save a job.

Job Details

Senior Associate Regulatory Affairs

Global Biopharmaceutical company

£31.07 per hour maximum pay

12 month contract

Uxbridge site - home working flexibility expected

ASAP start

37.5 hours per week

APPLICANTS MUST BE UK BASED UPON APPLICATION - YOU MUST HAVE THE RIGHT TO WORK IN THE UK TO BE CONSIDERED

Description

The Regulatory Professional under the direction of a Regional Regulatory Lead will assist in the creation and submission of regulatory documents and may be the regulatory lead for a program under the supervision of a more experienced regulatory lead.

Assist Regional Regulatory Lead to support regional regulatory pre-filing activities (e.g. core CTA/IMPD development and submission, support for pre-MAA filing, regulatory authority meeting preparations).

Provide and maintain CTA/MA documentation support (e.g. variations, substantial amendments, PDCO annual reports) in collaboration with Regional Regulatory Lead

Create and maintain product regulatory history documents through IMR/rRISE and appropriately archive all regulatory documents and agency communications.

Review regional component of the Global Regulatory Plan and provide input to operational deliverables.

Ensure compliance via timely submissions to regulatory agencies.

Support RRL in review of promotional materials for commercial activities (ex-US).

Collaborate with CROs / partners to support site initiation.

Coordinate collection of functional documents in support of regulatory applications.

As appropriate participate in GRT to support execution of regulatory strategy.

Coordinate QC of regulatory documentation (e.g. briefing packages).

Provide primary authorship to routine regulatory correspondence (e.g. annual reports, investigator packages).

Prepare regulatory packages and cross-reference letters to support investigator initiated studies

Approve drug shipment for Investigator Initiated Studies.

Complete regulatory forms to support agency communications (E.G. EudraCT,)

Provide regulatory support to Commercial, Medical and Clinical departments through cross-functional interactions in brand and therapeutic area teams.

Support process improvement initiatives, standards development, and metrics Assist in template development and maintenance.
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert