Due to changes in GDPR and increased usability with the website, any candidates registered before 03/05/19 will need to re-register
Hyper Recruitment Solutions
Back to results

Study Manager

Rushden, Permanent
Experience Dependant
Job Reference: J5631539
Updated On: 20/05/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Contract Research Organisation, Life Sciences, Science

Skills: Life Sciences - DMPK in vivo

Job Information

Role Overview

We are currently looking for a Study Manager to join a leading pharmaceutical company based in the Northamptonshire area. As the Study Manager in Metabolism you will be responsible for directing a range of studies for the development of new pharmaceutical products.

Key Duties and Responsibilities

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

1. You will be responsible for the execution of experimental work within the Metabolism department, ensuring the studies are completed within the timelines.

2. It will be your job to plan the work within the department, prepare study plans, make any adjustments in response to issues and file notes and deviations as required.

3. As the Study Manager, you will be required to communicate with people, internally and externally, as well as supervise and mentor more junior members of staff.

4. You will review the costs required for studies alongside the Team Leader by tracking actual and budgeted hours.

Role Requirements

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

1. A relevant degree in a science subject (e.g. Chemistry, Biochemistry, Biomedical Sciences, Pharmaceutical Sciences, etc.) is essential.

2. Proven industry experience in a Metabolism environment working to GLP regulations is necessary for this role. It is highly beneficial to have previous experience as a Study Manager.

3. A working knowledge and practical experience with in vivo studies, dose formulation and assessment, sample extraction and HPLC analysis is required for this role.

Key Words: Study Manager | Metabolism | CRO | GLP | Study Director | Project Management | Clinical | Non-Clinical | Biopharmaceutical | Pharmaceutical | Product Development | ADME | Biologics | Dermal
Georgina Beer
Your Recruitment ConsultantGeorgina Beergeorgina.beer@hyperec.com
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.