Clinical Research Executive - Hybrid working - Home based/remote

circa £40,000 plus benefits and remote working - Pharmacy roles
Ref: 511 Date Posted: Monday 05 Dec 2022
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Newton Blue is the on-site recruiter for some of the UK's leading tech and healthcare companies, including THIN, looking to recruit an experienced Clinical Research Executive.
 
"We're THIN, The Health Improvement Network (THIN), a real-world research service supporting retrospective and prospective clinical research studies. Part of the global Cegedim Group we've been providing research services to the wider healthcare and life sciences community since 1994 with the THIN database being  cited in over 1900 scientific research papers worldwide. We collect anonymised patient data from GP practices who are keen to participate in research across the UK and several European Countries. Our records span nearly 30 years with millions of anonymised Electronic Health Records immediately accessible to our trusted partners and collaborators"
Your next role?
Working with THIN and Cegedim Health Data (a division of the Cegedim Group) teams to create engagement opportunities with clinical research networks. You’ll be responsible for supporting and engaging our Health Provider Partners (GP Practices) to contribute towards research, bringing to the team a deep understanding of how to effectively set up and recruit sites within primary care into studies. 
The role will be focused on how to leverage both existing and new members in projects such as Pragmatic (Data Driven) Clinical Trials and Primary Market Research, seeing you managing some of the existing key accounts. 
  • Build relationships with clinical research networks throughout England
  • Build and own relationships with Health provider partners for specific studies (GP Practices)
  • Client account and project management
  • To assist in the management of the conduct of clinical trials and implementation of post-authorisation requirements.
  • To conduct remote monitoring in accordance with the protocols, GxP guidelines, applicable local and international regulations and company SOPs
  • To ensure subjects rights, well-being, data reliability and audit readiness
  • Site setup and operational training for projects (Including Clinical Trials)
  • Delivery of data accuracy through CRF review through remote monitoring according to the risk-based monitoring plan to ensure patient safety, compliance and decreased risk
  • In-house document quality management (including, but not limited to, trial master file, investigator site file)
  • Site setup, initiation, close-out and management (including monitoring) of sites participating in clinical and post-authorisation studies on an as needs basis
  • Draft report templates and define data tabulations required to support report development
  • Day-to-day project management to ensure project milestones are met and clients receive regular project status updates
  • Development of final study reports in PowerPoint and/or support of interactive dashboard design and co-ordination (where required)
  • Participation in investigator meetings and other Company meetings as necessary
What can we offer
  • Competitive salary
  • Hybrid mix of home and office work
  • Good benefit package
  • Progressive, quality driven business and people who believe in the benefits their work delivers to patient outcomes and the health of the UK population 
Are you what we're looking for?
We're looking for someone who has worked in a similar role, with great relationship building skills and an analytical, practical approach. With a Master’s/Bachelor’s degree or equivalent (preferably in physical, natural or biological science, medical disciplines, mathematics, economics or business) with previous experience in healthcare (NHS) or pharmaceutical research 
  • Experience in setting up and recruiting (investigator sites/patients) into Clinical trials (Pragmatic/Data driven) 
  • Ideally knowledge of Good Clinical Practice (GCP) and Regulatory guidelines 
  • Clinical research network engagements  experience 
  • Able to adapt, organize, prioritize, and work effectively in multi-functional teams in a constantly changing environment with a high level of initiative 
  • You have the ability to juggle multiple client / customer interactions and deadlines simultaneously and able to develop relationships and influence a diverse set of cross-functional stakeholders
  • Interest in consulting, healthcare in general, and the pharmaceutical industry