This job has expired

Study Nurse Education, South Korea - L

Employer
CROMSOURCE
Location
South Korea
Salary
Competitive
Start date
4 Dec 2023
Closing date
3 Jan 2024

Job Details

Description:

Location: South Korea - site based

Schedule: Freelance - Flexible 0.5 - 1FTE

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it's the best of both worlds....

TalentSource Life Sciences (the sponsor-dedicated division of CROMSOURCE, a ClinChoice company), is searching for a Study Nurse Education to join one of our sponsors in South Korea. This will be for between 0.5- 1 FTE, initially for 24 months.

CROMSOURCE is an international CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with their client counterparts.

The Study Nurse will provide patient and carer training and support on the correct deployment and patient use of the Duodopa pump system, including practical training and handling for Neurologists, Gastroenterologists, Radiologists, nurses and other members of the healthcare team. In addition, the Study Nurse will provide practical and technical support.

Main Job Tasks and Responsibilities:
  • Ensure correct and appropriate level of understanding for the deployment and use of the DuoDopa pump.
  • Develop relationship with Investigators and study site teams for the deployment of the Duodopa pump in the context of clinical trials.
  • Assist in the conduct of patient feasibility, Patient Pathway Mapping and the implementation and ongoing assessment of Parkinson's disease patient recruitment strategies at the investigator site level.
  • Confirm activation of Honorary Contract with study site before any work is undertaken. Ensure appropriate Honorary Contract is in place for the purpose of carrying out clinical trial duties at site. Renew contract when necessary.
  • Teach patient/carer, nursing and medical staff about the background, rationale and correct deployment of the DuoDopa pump. Assess and monitor patient/carer's understanding in relation to pump deployment and take corrective action as necessary.
  • Update the other members of the Parkinson's disease/Gastrology team and maintain a positive working relationship.
  • Liaise with Investigators in the collation of accurate feasibility and project status data in a timely manner.
  • Perform further training with patients where necessary, ensuring this is documented appropriately.
  • Attend the DuoDopa training Investigator Meetings/study meetings.
  • Play a pivotal role in the communication between the Parkinson's patient/carer, Investigator and Sponsor's representative and act as an ambassador of the Sponsor in all communications.
  • Update the Sponsor of any significant communications or of any changes to procedure; ensure this is documented appropriately.
  • Provide administrative and logistical support at site for the conduct of Clinical Trials at the discretion of the Sponsor and designated Investigator.
  • May facilitate Source Data Verification in accordance with the Investigator's direction.
  • May implement the use of eTechnology where appropriate and in accordance with procedures defined by the Sponsor.


Education, Experience and Skills:
  • Registered Nurse (RGN/RMN/RSCN or equivalent), Medical Physician or appropriate para-medical qualification and/or experience as accepted in accordance with local country requirements.
  • At least 2 years post-registration clinical experience.
  • Must have experience with clinical trials.
  • Previous experience with the DuoDopa pump is required.
  • Experience with nursing within surgery/neurology preferred but not mandatory.
  • Excellent communication and interpersonal skills; ability to talk with patient and their families/carers in a professional, courteous and empathetic manner.
  • Awareness of all relevant Health and Safety Procedures (clinical, surgery, patients home, etc.).
  • Willingness to travel as required.
  • Fluent in English and local language.


The Application Process

Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs please contact mailto:careers@cromsource.com for more information.

Who will you be working for?

About CROMSOURCE

CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: Study Nurse, Nurse, Study Nurse, Clinical Research Nurse, Clinical Study Nurse, Research Nurse, Clinical Nurse, Registered Nurse, Freelance, FL, Contract, Temporary, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated

Skills:

Freelance, Nurse, Nurse Manager, Registered Nurse, Clinical Research Organisation, Contract, CRO, Outsourcing

Location: South Korea

Share:

LinkedIn Facebook Twitter Email

Company

CROMSOURCE is now part of ClinChoice. Learn more about ClinChoice by visiting

ClinChoice

CROMSOURCE, a ClinChoice company, is an ISO-certified international provider of fully outsourced services to the pharmaceutical, biotechnology and medical device industries, specialised in clinical development and flexible resourcing solutions.

CROMSOURCE was founded in 1997 and its successful growth has been built on stability, integrity, and high levels of customer satisfaction. We have grown steadily through offices across all regions of Europe and North America and delivering a comprehensive breadth of services.

Acting through PharmaceuticalMedical Device and Flexible Resourcing Solutions teams, and with a comprehensive portfolio of services, we offer a flexible approach to ensure CROMSOURCE optimally supports the unique needs of each client. This could mean providing regulatory consultancy to a small company at the early stages of a medical device development programme, through to provision of full services to a pharmaceutical company performing an international mega-trial to support registration of their product. Whatever the size and scope of the project, each receives the same level of attention to detail and commitment to delivery of a high quality service within budget and to timelines agreed.

We are experts providing experts and we live by our motto – Advise Agree Deliver. This means we leverage our experience and expertise at the early stages of discussions with our clients to freely advise them on the optimal project plan. We then reach agreement with each client on the scope of service, timelines and budget. CROMSOURCE then commit to deliver those services on time and within budget – according to our End-to-End Guarantee and this commitment to guaranteed delivery is unique in the clinical research environment.

 

 

 

Company info
Website
Telephone
+44 (0) 1786 468990
Location
6-9 The Square
Stockley Park
Hayes
Uxbridge
UB11 1FW
United Kingdom

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert