Clinical Research Recruitment
What is Clinical Research?
Clinical Development
Clinical Development involves collaboration with various stakeholders such as medical professionals, regulatory bodies and patients. In addition, it requires extensive knowledge of the drug development process, including clinical trial design, data analysis and interpretation. Also, they are responsible for designing, planning and executing Phase I to Phase III clinical trails. As well as Phase IV post-marketing surveillance.
Clinical Operations
This is key to the delivery of clinical trails in the drug development pipeline. Without this function, studies could not be effectively conducted. Professionals in this sector are responsible for designing, planning and executing Phase I to Phase III clinical trails. They are also responsible for Phase IV post-marketing surveillance.
Our Experience
We specialised in the clinical research space. Building a strong network of highly skilled professionals that trust in the Scienta brand. Thanks to our in-depth understanding of this particular area of recruitment, we know what skills to look for and how to engage with top talent.
Key Roles We’ve Filled
Senior Clinical Scientist
Senior Clinical Trail Manager
Senior Clinical Training Specialist
Current Clinical Research Roles
-
View job details
Quick apply
Permanent
Clinical Research
Clinical Scientist
Italy
Clinical Scientist
- Clinical Research
- Italy
- Permanent
Apply now
-
View job details
Quick apply
Contract
Clinical Research
Freelance Oversight Monitor
Japan
Freelance Oversight Monitor
- Clinical Research
- Japan
- Contract
Apply now
-
View job details
Quick apply
Permanent
Clinical Research
Senior Director Clinical Development – Diabetes
United States
Senior Director Clinical Development – Diabetes
- Clinical Research
- United States
- Permanent
Apply now
Our Experts
Nathan McGovern
Principal Consultant
Clinical Operations – Contracts
I have 8+ years supporting Pharma, Biopharma and Biotech companies for their resource requirements across Europe and the USA. Interim and Freelance assignments at varied FTE.
My therapeutic understandings include, but are not limited to; Oncology, Immuno-oncology, Cardiovascular, Neurology, Immunology and Gene and Cell Therapy.
Katie Bowser
Recruitment Consultant
Clinical Operations
I support the build-out of Clinical Operations teams across the European and US biopharma industries. My network includes experienced professionals across the following functions:
Clinical Operations
Study Management
Business Operations
Vendor Management
Trial Optimization
Study Start-Up
Site Management
Speak to Our Experts
Frequently Asked Questions
How do I become a clinical research associate?
To become a Clinical Research Associate (CRA) you will need an undergraduate or postgraduate qualification in one of the following fields:
- Nursing
- Biology
- Microbiology
- Toxicology
- Biochemisty
- Pharmacology
- Physiology
- Immunology
- Medicine
- Anatomy
- Pharmacy
Also, if you’re looking at your more longterm career progression, it’s recommended to get a PhD in one of those areas.
Additionally, if you’re an employer, have you considered training rather than competing for talent? Icon have created a great free white-paper
What does a clinical research coordinator do?
They are a healthcare professional who organises and performs medical research. They also manage clinical trials to test drugs for effectiveness and safety.