Phoenix Clinical Research is Looking for a Freelance Research Nurse in Lebanon
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Phoenix Clinical Research is Looking for a Freelance Research Nurse in Lebanon

15:30 06 September in Career, News


The Research Nurse (RN) ensures that the clinical trials are carried out according to the protocol, local regulations and the followed guidelines, such as Good Clinical Practice (GCP), Good Documentation Practice (GDP), etc.

The RN must be trained on the applicable SOPs, study requirements, supporting documents, procedures, and timelines to ensure proper administration of the study drug to the patient and to do the proper follow-up on the safety and well-being of the patient during the study conduct.

Location: Lebanon

Contract: Freelance

Principal Duties and Responsibilities:

• Communicate effectively with the project team and the Principal Investigator (PI), to ensure a smooth and efficient flow of information

• Maintain accurate documentation as per the SOPs followed in the project

• Ensure subject confidentiality and adherence to GCP

• Ensure compliance with the data protection requirements

• Attend Site Initiation Visits (SIV) as required and any other necessary meetings

• Coordinate and complete subject trial visits on- and off-site

• Ensure all trial related procedures and assessments are completed according to the protocol and relevant SOPs

• Administer trial medication as per the protocol, and facilitate the safe storage, transfer and patients’ accountability

• Process and safely pack and dispatch samples, liaising with courier companies as needed

• Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials providing information and support for patients for on- and off-site care

• Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team

• Report any suspected misconduct or fraud

• Assist the PI in the consenting process as per the site delegation log

• Assist with the maintenance of Investigator Site Files as assigned by the study team/ project manager

• Understand and comply with the relevant local hospital policies and guidelines

• Provide support to obtain regulatory approvals e.g., completion and submission of Research Ethics Committee applications and amendments and local site approvals.

Required Qualifications & Documents:

Verification of Identity Two forms of identity, one of which must be photographic and one of which must show current address
Proof of right to work in the country
Professional current and in date nursing registration and qualification checks
Relevant Nursing employment experience via personal CV
Details of two work related employment references
Details of Emergency Contact
Criminal record check within the last 3 years
GCP certification undertaken within the last 2 years
Occupational Health documentation in relation to all relevant immunisations specific to country requirements including Hepatitis B.  
Valid driving licence
Valid car insurance documentation, ensuring cover for business use (if applicable locally).
Basic life support training
IATA training (Handling dangerous goods) certification
Infection control training certification
Manual handling training certification

If you are interested, you can send your CV on: