Research Analyst
- Brentford, Greater London (GBR)
- £700 - £710 Per Day
- 12 Months
- Start date: ASAP
- Ref: GSK0JP00099188
- research
- clinical trial
- analytical test methods
- pharmaceutical
- sops
- regulatory
- validation
- fda
- epidemiology
- degree
GSK: GSK0JP00099188
Job Title: Research Analyst
Rate: £710.00 Umbrella
Location: Remote
Duration: 12 months
Who Are We - GSK?
We are a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. GlaxoSmithKline plc was formed in 2000 as a result of a merger between Glaxo Welcome plc and SmithKline Beecham plc, although our history can be traced back more than 300 years to London’s Plough Court Pharmacy in the 1700s.
Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. Our strategy is to bring differentiated, high-quality and needed healthcare products to as many people as possible, with our three global businesses, scientific and technical know-how and talented people. Our values and expectations are at the heart of everything we do and form an important part of our culture:
• Our values are Patient focus, Transparency, Respect, Integrity
• Our expectations are Courage, Accountability, Development, Teamwork
Role purpose / summary
We are currently recruiting for Research Analyst to
join our Quality Control team at the Worthing Manufacturing site. The role(s) carry out physical and chemical analytical test methods on oral, stability and sterile products using SOPs, and accurately document the results as part of the Quality Control process to ensure a batch of product is of satisfactory quality for release to the market.
Key Skills/ requirements
Essential:
· Experience with planning and managing PRO development and validation projects
· Clear understanding of the FDA Patient Reported Outcomes Guidance
· Experience in pharmaceuticals, particularly in drug and vaccine development, with demonstrated experience in clinical trial planning and execution
Desirable:
· Strong background in statistical methods for the evaluation of PROs/COA endpoints.
· Understanding of healthcare markets and regulatory and reimbursement decision making, especially in relation to the global use of PRO data in drug and vaccine development.
· Understanding of the evolving methods and regulatory environment with respect patient-reported outcomes (PRO) and clinical outcome assessments (COA)
· Strong verbal and written communication skills, with stakeholder engagement from operations through executive levels
Basic Qualifications
· Master’s or Doctoral degree in Psychology, Psychometrics, Social Sciences, Outcomes Research, Health services research, Public Health, Epidemiology, Pharmacy, or a closely related discipline
· Minimum 7 to 10 years of experience in a related role, including demonstrated experience with PRO/COA development and implementation in a consulting and/or pharmaceutical company environment
When applying for this role, please use your CV to describe how you meet the competencies for this role, as outlined in the job requirements above.
The information that you provide in your cv will be used to assess your application
All profiles will be reviewed against the required skills and experience. Due to the high number of applications we will only be able to respond to successful applicants in the first instance. We thank you for your interest and the time taken to apply!
Join GSK’s vision to do more, feel better and live longer:
https://www.youtube.com/user/gskvision/
Who will I be working with?
http://www.gsk.com/en-gb/careers/meet-our-people/
