Clinical Operations Leader (hybrid)
- Recruiter
- Hobson Prior
- Location
- Welwyn Garden City
- Salary
- Competitive
- Posted
- 01 Aug 2022
- Closes
- 17 Aug 2022
- Sectors
- Scientific & Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
Hobson Prior are currently seeking a Clinical Operations Leader to join a brilliant pharmaceutical corporation on a contract basis inside IR35 with hybrid working available. Our client is focused on producing ground-breaking remedies for various therapeutic areas.
Please note that to be considered for this role you must have the right to work in this location.
Key Responsibilities:
For this role, you will handle relations suppliers and shareholders.
Monitor performance of suppliers and third-party vendors.
To guarantee sites have the essential resources to run clinical trials, you will plan demand and supply by supervising the resource management, forecast and maintenance of resources required.
You will drive operational brilliance by evolving operational plans, producing and handling clinical study budget and supervising the consistency of operations.
The ideal candidate will handle risk and conformity by evolving site monitoring and risk mitigation tactics and guarantee the team adhered to all suitable standards which involves ICH/GCP and any other guidelines.
To warrant countries and sites are selected for contributing in trials, you will offer country oversight by guiding feasibility examinations.
Any other assigned duties.
Key Skills:
Eager to accomplish successful results and deliver throughout assignment.
A self-starter who is talented and passionate, as well as motivated by the company's mission.
Works well in a team environment with a rigorous and entrepreneurial spirit.
Possess a growth outlook.
You are comfortable thinking on your feet and thrive in a fast-paced, ambiguous setting.
Requirements:
At least 3 years of experience in a pertinent position, or a clinical trial management role which would be advantageous.
Educated to a degree level in a life science discipline or pertinent work experience.
Focused on quality service delivery for PDG throughout the assignment.
Knowledge of drug development procedures and respective guidelines, which involves ICH and GCP regulations.
Apply now :
If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
Please note that to be considered for this role you must have the right to work in this location.
Key Responsibilities:
For this role, you will handle relations suppliers and shareholders.
Monitor performance of suppliers and third-party vendors.
To guarantee sites have the essential resources to run clinical trials, you will plan demand and supply by supervising the resource management, forecast and maintenance of resources required.
You will drive operational brilliance by evolving operational plans, producing and handling clinical study budget and supervising the consistency of operations.
The ideal candidate will handle risk and conformity by evolving site monitoring and risk mitigation tactics and guarantee the team adhered to all suitable standards which involves ICH/GCP and any other guidelines.
To warrant countries and sites are selected for contributing in trials, you will offer country oversight by guiding feasibility examinations.
Any other assigned duties.
Key Skills:
Eager to accomplish successful results and deliver throughout assignment.
A self-starter who is talented and passionate, as well as motivated by the company's mission.
Works well in a team environment with a rigorous and entrepreneurial spirit.
Possess a growth outlook.
You are comfortable thinking on your feet and thrive in a fast-paced, ambiguous setting.
Requirements:
At least 3 years of experience in a pertinent position, or a clinical trial management role which would be advantageous.
Educated to a degree level in a life science discipline or pertinent work experience.
Focused on quality service delivery for PDG throughout the assignment.
Knowledge of drug development procedures and respective guidelines, which involves ICH and GCP regulations.
Apply now :
If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.