Analyst – Regulatory Information management

Description

Job Title: Analyst – Regulatory Information Management

Location: Marlow

Contract: 12 Months / Hybrid 3 days onsite

Hours: 37.5 hours per week

Rates: 23 p/h

Job Description

SRG are looking for an analyst – regulatory information management for a leading pharmaceutical company based in Marlow. As part of this role, you will be supporting process improvement initiatives. Support structured data submissions and all related tasks, including xEVMPD, SPOR and IDMP implementation.

Support Regulatory Information Management (RIM) globally, focusing on key systems and processes, including COSMOS (RIM system) Supports Data enrichment and archiving remediation initiatives.

Work with members of the Regulatory Lifecycle Management team to share knowledge and improve RIM processes.

Build and maintains relationships with Regulatory and other staff within and outside of the region to ensure effective communication and efficient implementation of regulatory information management.

Duties and Responsibilities

Subject to internal QC audit, ensure all data submissions and related reference/master data are managed accurately and in accordance with SOPs.Establish relationships with 'in–country' teams and global regulatory teams to ensure that they are aware of how data submissions are managed.Maintain awareness of International regulatory procedures and how any changes may impact reference and master data management within the Regulatory Information Management system.Work with other Local System Administrators to suggest, discuss and implement system and process improvements in line with regulatory changes and as part of a quality management cycle, subject to Global Data Council representations and approvals. Work with global BTS to implement system upgrades and other improvements.Qualify requests and run accurate reports and queries as requested.Maintain compliance with departmental SOPs and Work Instructions.

Experience and Qualifications

Graduate (preferably in a Life Science or IT related discipline), or equivalent/relevant experience.Knowledge of Regulatory Business Processes / Pharma and/or Medical Devices R&D BusinessRegulatory Systems and Database experience (Liquent, Veeva, CARA or similar)Some knowledge of European Regulatory Procedures (Centralised, Decentralised and Mutual Recognition)Some knowledge of Regulatory Submission types (MAAs, Variations, Renewals, CTAs, DSURs etc)Knowledge of EMA Platforms preferred (IDMP, XEVMPD, SPOR, CTIS, IRIS)

Essential Skills and Abilities

Organisational and planning abilityExcellent written, verbal and interpersonal skillsAbility to work effectively and collaboratively across cultures and cross–functionallyAbility to identify compliance risks and escalate when necessaryAbility to multitask, prioritize, and manage multiple projects and deadlinesSense of personal responsibility and accountabilityCarbon60, Lorien & SRG – The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Ad ID: 5416968574