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Life Science jobs in United Kingdom

Director, Feasibility

Medpace

London
On-site
GBP 80,000 - 120,000
30+ days ago
I want to receive the latest job alerts for “Life Science” jobs

GxP Validation Engineer/Analyst (Lab Equipment)

ZipRecruiter

Cambridge
On-site
GBP 40,000 - 60,000
30+ days ago

Project Architect- Life Science

ZipRecruiter

London
On-site
GBP 40,000 - 70,000
30+ days ago

Crop Trials Research Assistant

Menter a Busnes

West Midlands Combined Authority
On-site
GBP 26,000 - 29,000
30+ days ago

Senior Analytical Scientist

taylorollinson Ltd

United Kingdom
On-site
GBP 35,000 - 50,000
30+ days ago
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Actemium Automation Teesside - Business Development Manager

VINCI

Stockton-on-Tees
On-site
GBP 55,000 - 70,000
30+ days ago

Actemium Automation Teesside - Senior Software Controls Systems Engineer

VINCI

Stockton-on-Tees
On-site
GBP 50,000 - 55,000
30+ days ago

Senior Consultant, VAT/Indirect Tax | Corporate Finance & Restructuring

FTI Consulting

London
Hybrid
GBP 50,000 - 80,000
30+ days ago
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Senior Clinical Data Manager - UK/EU - Remote

Worldwide Clinical Trials

United Kingdom
Remote
GBP 30,000 - 60,000
30+ days ago

Planner - Infrastructure

ZipRecruiter

London
On-site
GBP 40,000 - 80,000
30+ days ago

Pharmacy Manager Bradford

Resourcing Life Science

Bradford
On-site
GBP 80,000 - 100,000
30+ days ago

Relief Pharmacist UK

Resourcing Life Science

United Kingdom
On-site
GBP 80,000 - 100,000
30+ days ago

Medical Service Engineer UK

Resourcing Life Science

United Kingdom
On-site
GBP 80,000 - 100,000
30+ days ago

Citrix System Engineer UK

Resourcing Life Science

United Kingdom
On-site
GBP 80,000 - 100,000
30+ days ago

IT Network Security Engineer Pharma UK

Resourcing Life Science

United Kingdom
On-site
GBP 80,000 - 100,000
30+ days ago

Commercial Life Science MEP Lead

AECOM

St Albans
On-site
GBP 50,000 - 90,000
30+ days ago

VP, MDS Digital & Knowledge Management

GSK

Stevenage
Hybrid
GBP 100,000 - 150,000
30+ days ago

Bioinformatics Engineer I

Exact Sciences

England
On-site
GBP 30,000 - 45,000
30+ days ago

Bioinformatics Engineer I

Exact Sciences

Oxford
On-site
GBP 30,000 - 45,000
30+ days ago

Finance Business Partner (M/F/D)

Avantor

Lutterworth
Hybrid
GBP 50,000 - 75,000
30+ days ago

Pathology Research Technician (M/F/D)

Avantor

Cambridge
On-site
GBP 25,000 - 45,000
30+ days ago

Digital Marketing Specialist, SEM

Avantor

Reading
On-site
GBP 35,000 - 50,000
30+ days ago

Digital Marketing Specialist, SEM

Avantor

Basingstoke
On-site
GBP 35,000 - 50,000
30+ days ago

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Director, Feasibility
Medpace
London
On-site
GBP 80,000 - 120,000
Full time
30+ days ago

Job summary

A leading clinical research organization is seeking a Director, Feasibility, who will assess new clinical trial opportunities. This role requires a strong clinical background and expertise in trial management, driving collaborations across teams to enhance study efficiency globally.

Benefits

Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Qualifications

  • 5-7 years of project management/clinical trial management/feasibility experience in clinical research.
  • Thorough knowledge of feasibility processes.
  • Advanced understanding of operational aspects of clinical trials.

Responsibilities

  • Evaluate and support new clinical trial opportunities.
  • Work strategically with Medical Experts and Regulatory Submissions team.
  • Collaborate with Investigators and country managers.

Skills

Analytical thinker
Attention to detail
Leadership
Communication

Education

Bachelors degree
Masters/PhD preferred
Job description

Responsibilities

We are currently seeking a Director, Feasibility, who will be an integral team leader within our global Proposals and Feasibility team. This position will evaluate and support new clinical trial opportunities by working strategically with Medpace Medical Experts, Clinical Trial Managers and our Regulatory Submissions team. By collaborating with Investigators and international country managers, as well as analysis of multiple data sources, this individual will strategize the most efficient scenario to conduct various studies globally. If you are an individual with a strong clinical background and expertise in clinical trial management, please review the following career opportunity.


Qualifications

  • Bachelors required, Masters/PhD preferred
  • 5-7years of project management/clinical trial management/feasibility experience in clinical research, CRO experienced preferred
  • Analytical thinker with great attention to detail
  • Thorough knowledge of feasibility processes
  • Advanced understanding of operational aspects of clinical trials
  • Ability to work independently
  • Outstanding leadership, and communication skills

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 4,000 people across almost 40 countries.


Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

Awards

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets

  • Bachelors required, Masters/PhD preferred
  • 5-7years of project management/clinical trial management/feasibility experience in clinical research, CRO experienced preferred
  • Analytical thinker with great attention to detail
  • Thorough knowledge of feasibility processes
  • Advanced understanding of operational aspects of clinical trials
  • Ability to work independently
  • Outstanding leadership, and communication skills

We are currently seeking a Director, Feasibility, who will be an integral team leader within our global Proposals and Feasibility team. This position will evaluate and support new clinical trial opportunities by working strategically with Medpace Medical Experts, Clinical Trial Managers and our Regulatory Submissions team. By collaborating with Investigators and international country managers, as well as analysis of multiple data sources, this individual will strategize the most efficient scenario to conduct various studies globally. If you are an individual with a strong clinical background and expertise in clinical trial management, please review the following career opportunity.

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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