Regulatory Scientist

CK Group; Bracknell; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A large pharmaceutical company is seeking a Regulatory Scientist to join their team in Bracknell on a contract basis for 12 months. The role involves providing support on regulatory submissions, engaging with cross-functional partners, and ensuring compliance with regional protocols. Candidates should possess a relevant scientific degree and 1-3 years of industry-related experience. The position offers a competitive hourly salary and a flexible work arrangement of three days on-site and two days working from home.

Qualifications

• Bachelor with 1 or 2.1 honours, Master’s with distinction or merit, or PhD in a relevant scientific subject.
• Industry-related or other relevant work experience (1-3 years).
• Knowledge of local/regional regulatory procedures and practices.

Responsibilities

• Provide input and review of global strategic plans and regional submission documents.
• Support Regional Regulatory Lead Scientist during governance committees.
• Ensure delivery of content for local regulatory submissions.

Skills

Knowledge of local / regional regulatory procedures

Ability to assess and propose risk management strategies

Knowledge of the drug development process

Education

Bachelor or Master’s or PhD in a relevant scientific subject

Job description

Regulatory Scientist

CK Group are recruiting for a Regulatory Scientist

to join a company in the pharmaceutical industry on a contract basis for 12 months.

Salary: £14.68-£19.15 per hour PAYE

Responsibilities

• Provide region / country input and review of global strategic plans and global / regional submission plans and documents.
• Provide support to Regional Regulatory Lead Scientist during key governance committees on regional regulatory strategy decisions, if requested (e.g. when key discussion topics impact the region).
• Ensure approval and delivery of content for local regulatory submissions, engaging cross functional partners in contributing to development of submission content.
• Provide support to Regional Regulatory Lead Scientist for meetings and interactions with regulators in assigned region and engage cross functional partners to contribute to regulator interactions.
• Support development of local / regional labelling strategy (product information and packaging) and help to network for alignment across region / affiliate team to enable timely completion of registration milestones.

Qualifications

• Bachelor with 1 or 2.1 honours, Master’s with distinct or merit or PhD in a relevant, scientific subject.
• Industry-related or other relevant work experience (1-3 years).
• Knowledge of local / regional regulatory procedures and practices.
• Knowledge of the drug development process.
• Ability to assess and propose ways to manage risk in a highly regulated environment.

Company

Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs.

Location

This role is based at our clients site in Bracknell (3 days on site, 2 days work from home).