Celerion

Clinical Conduct Associate (Medical Research)

Celerion  •  Belfast, GB (Onsite)  •  3 hours ago
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Job Description

Every member of the Celerion team is involved in making something essential – a distinctive contribution to the health and well-being of people around the world. That’s the sense of purpose shared by employees throughout Celerion. We are an early phase drug research company, operating in robust and growing markets. We have an exciting future and offer a strong development environment for our excellent employees.

We are looking for Clinical Conduct Associates to join the clinical conduct team at our Phase I clinical trial facility in Belfast, N. Ireland.

The responsibilities of this technical position include collecting safety data such as vital signs, recording ECGs, assisting with urine and blood draw collections, serving meals to study participants and collecting raw data using an electronic data capture system.

Full-time (37.5hr/week) positions are available. Salary will increase with completed skills training modules and the benefits package includes holidays, pension, life assurance, income protection insurance and private medical insurance.

Requirements

  • Candidates must be educated to GCSE level (any grade) with 2+ years’ work experience ; or have 2+ years experience in Band 3 in healthcare; or have completed A Levels or BTEC/NVQ in healthcare (Full training in clinical research technical skills will be provided)
  • This is a full-time position with variable working hours and shift pattern. The shift pattern includes week days, weekends and also night shifts once training has been completed so applicants must be fully flexible to working hours.
  • Excellent interpersonal skills are also required. This role is very team orientated with a high professional attitude expected.

Celerion is an equal opportunities employer.

Celerion

About Celerion

Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines.

With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings.

Our operations are strategically located in:

Lincoln, Nebraska (Corporate Headquarters)

Philadelphia, Pennsylvania

Phoenix, Arizona

Belfast, Northern Ireland,UK

Zurich, Switzerland

Vienna, Austria

Richmond, Virginia

Montreal, Quebec, Canada

For more information, visit: www.celerion.com

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Lincoln, NE
Year Founded
2010
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