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Biotech 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 “Biotech” jobs

AI Engineer

MEDPACE

London
On-site
GBP 50,000 - 85,000
30+ days ago

UKRI Procurement Manager

UK Research and Innovation

East Hagbourne
Hybrid
GBP 39,000 - 45,000
30+ days ago

Founding Frontend Engineer

Solve Intelligence

England
On-site
GBP 50,000 - 75,000
30+ days ago

Research Associate in Regional Plastics & Chemical Systems Decarbonisation

International Society for Industrial Ecology

Sheffield
On-site
GBP 38,000 - 47,000
30+ days ago
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Professor of Practice in Biomedical Engineering

Clarkson University

Weston-super-Mare
Hybrid
USD 85,000 - 120,000
30+ days ago

Environmental Health & Safety Specialist *PC 834

Miltenyi Biotec Inc

East Hampshire
On-site
USD 102,000 - 139,000
30+ days ago

Biotechnology Patent Attorney - Qualified - CPA/EPA - Tier 1 Firm

EJ Legal

London
On-site
GBP 60,000 - 100,000
30+ days ago
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Patent Attorney - Biotechnology - Qualified - Tier 1 Firm

EJ Legal

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

Member of Product & Partnerships Counsel

Solve Intelligence

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

Finance Officer

ORYX BIOTECH LTD

United Kingdom
On-site
GBP 60,000 - 80,000
8 days ago

Medical Affairs Strategic Lead

Singular Biotech

London
Remote
GBP 125,000 - 150,000
11 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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