Clinical Research Nurse

JR United Kingdom; Middlesbrough; On-site; GBP 35,000 - 55,000; Full time

Job summary

A leading clinical staffing firm is seeking a Freelance Clinical Research Nurse to support urgent studies in York. The ideal candidate should be NMC registered, with experience in fast-paced healthcare settings and must possess a full driving license to travel between sites.

Qualifications

• Experience in a fast-paced environment preferred.
• Must be NMC registered with a full driving license.
• Immediate starters preferred due to urgent needs.

Responsibilities

• Support ongoing studies in York on a permanent basis.
• Utilize clinical expertise to improve the recruitment process for clinical trials.

Skills

Clinical Research

Fast-paced environment

Education

NMC Registration

Job description

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The company has experienced an 18% growth over the past 2 years and is using this success to further their mission of connecting patients to clinical trials through recruitment and retention activities. Founded by industry experts, they leverage digital technologies to improve the reach and accessibility of clinical trials.

The Role

We are seeking a Freelance Clinical Research Nurse to support ongoing studies in York on a permanent basis. The ideal candidate must be NMC registered, have experience in a fast-paced environment, and possess a full driving license to support travel between sites. Immediate starters are preferred due to urgent needs.

Requirements

• NMC registered
• Experience in a fast-paced environment
• Full driving license

About Planet Pharma:

Planet Pharma is an American parented employment business and agency providing global staffing services. Headquartered in Chicago with an EMEA regional office in Central London, we operate in over 30 countries with a network of more than 2,500 active contractors worldwide. We offer both contract and permanent recruitment services.

Recognized by FORBES as the 17th best professional staffing firm, we have received multiple industry awards for excellence and service. Our expertise spans Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions, Clinical Development, Quality, Biostatistics, and Medical Affairs/Writing.

We are committed to equal opportunity employment and welcome applications from all qualified candidates regardless of race, sex, disability, religion/belief, sexual orientation, or age.