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LC-MS Study Director

North YorkshirePermanent
£30,000 - £45,000 per annum
Job Reference: J5633042
Updated On: 04/03/2020
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Contract Research Organisation, Contract Testing Organisation, Life Sciences

Skills: Chemistry - Analytical - LCMS, Chemistry - Analytical - Instrument Validation

Job Information

Role Overview

Are you an experienced Study Director within Bioanalysis looking for a new exciting opportunity?

We are currently looking for a LC-MS Study Director (Bioanalysis) to join a global scientific company in the York area.

As the LC-MS Study Director you will be responsible for the scientific, technical and regulatory conduct of Bioanalytical studies and the interpretation, documentation and reporting of results.

Key Duties and Responsibilities

Your duties as the Study Director will be varied however the key duties and responsibilities are as follows:

1. You will provide Project Leader support, scientific and regulatory oversight for the conduct of a wide variety of bioanalytical GLP / GCP pre-clinical and clinical validation projects and pre-clinical and clinical sample analysis projects.

2. You will work closely with other Scientists and Project Leaders to ensure that study work is performed in accordance with relevant technical and quality GLP standards and is delivered in a timely and cost-effective manner.

3. You will liaise and communicate with your clients and ensure all study plans and reports are delivered on time. You will work closely with QA to ensure audit comments are closed in a timely manner. You will work closely with Business Development executives in the production of quotes and invoices.

4. Additionally, as the LC-MS Study Director within Bioanalysis, you may also be involved in the quantitative bioanalysis using UPLC-MS/MS and plate based technology when required.

Role Requirements

To be successful in your application to this exciting opportunity as the Study Director we are looking to identify the following on your profile and past history:

1. Relevant scientific degree (BSc, MSc or ideally a PhD).

2. Proven industry laboratory experience in bioanalysis as well as experience being in the similar role as study director or project leader under GLP regulations is essential for this role.

3. You must also be highly organised with the ability to effectively prioritise your workload.
Debra Fong
Your Recruitment ConsultantDebra
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.