Labcorp Drug Development Job - 39673665 | CareerArc
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Company: Labcorp Drug Development
Location: England, United Kingdom
Career Level: Entry Level
Industries: Healthcare, Pharmaceutical, Biotech


Job Overview:

Do you have experience of Client Study Management and looking for your next opportunity to join a rapidly expanding team?


Are you interested in developing your career with management responsibility?


Do you want to be a part of the world's leading drug development company?


Our largest UK site in Harrogate, North Yorkshire is currently recruiting for a QC Scientist/Study Manager/Director to join the CMC (Chemistry, Manufacturing Controls) division and will be responsible for the managing of batch testing, release testing, sample analysis, stability, assay development, assay establishment or validation/transfers with monoclonal antibodies.  This role is looking for previous experience with qPCR and DNA extraction.


Labcorp Drug Devlopment has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today. Chances are, you or someone you know has benefitted from a medicine or medical device that Labcorp Drug Development helped develop.


What Labcorp Drug Development can offer you:

  • Competitive salaries and a comprehensive benefits package including health cover and contributory pension
  • Unrivalled opportunities to develop a successful career in the scientific industry, utilizing multiple analytical techniques
  • Unsurpassed career development opportunities, with the ability to develop your management skills
  • Ability to work with a variety of different clients on wide ranging projects
  • Opportunity to work in a rapidly expanding and leading edge field


Job responsibilities include:


  • Act as a Subject Matter Expert (SME) or Principal Investigator within BioCMC with knowledge of standard and non-standard study designs and the ability to draw scientific conclusions
  • Working method knowledge e.g. instruments used within the laboratories and ability to make decisions on assay results, suggest assay/technique advancements/improvements to the client, and follow through with the client as necessary
  • Assist in the preparation/review of training modules in areas of expertise and mentors and develops others in the group 
  • In-depth knowledge of study process from award to finalisation archiving and amendments to final reports and to write and review Analytical Procedures, Policies, SOPs and Guides where appropriate.
  • Employ effective general management, communication and interpersonal skills to work within the project teams, with the Client and other project stake-holders e.g. supporting functions at Labcorp Drug Development
  • Participate in client regulatory audits and perform revenue recognition where required
  • Responsible for on-time delivery of data, project documents, and quality documents

Relocation assistance may be available for this role


  • Join a supportive, diverse community of hard-working people who push new boundaries
  • Expand your expertise and open the door to many advancement opportunities within our global organization
  • Get ready to transform healthcare and change lives around the world
  • The post holder should ideally have a relevant degree along with industry experience
  • Technical expertise in at least one of the following scientific disciplines - eg qPCR, DNA extraction within Microbiology or Gene Therapy
  • Experience in similar types of study management and client management
  • An in-depth understanding of health and safety policies and a good understanding of GMP/GLP/GCP and an up to date knowledge of regulatory guidelines
  • Able to communicate effectively at all levels with internal employees and external clients, with the ability to get things done by influencing others
  • Commercial awareness, interpersonal and negotiating skills and able to learn and maintain knowledge of process excellence processes
  • Commercial awareness, interpersonal and negotiating skills

 Apply on company website