Research Nurse

Orion Group; York and North Yorkshire; On-site; GBP 25,000 - 32,000; Part time

Job summary

Orion Group Life Sciences is recruiting a Research Nurse for a multinational biopharmaceutical client in York on a 6-month contract with potential to extend. The role is 24 hours per week, typically spread over 3 days on-site at a GP practice in York, with weekday flexibility.

The position supports study sites in coordinating Phase I-IV trials, ensuring compliance with protocol, GCP, and regulations, while maintaining high nursing standards and patient safety.

Qualifications

• Bachelor's degree in Nursing with 1 year of relevant experience or equivalent
• Current active nursing license in the relevant jurisdiction
• Applicable certifications and licenses as required by regulatory bodies

Responsibilities

• Coordinate clinical research studies under supervision by a principal investigator
• Maintain current nursing skills and knowledge related to clinical research
• Safeguard volunteers' well-being and maintain high safety standards
• Support study conduct including protocol review, CRF review, and data capture
• Recruit and screen volunteers for study inclusion
• Orientate volunteers to the study purpose, procedures, and visit timelines
• Administer and custody of study drug per SOPs
• Perform procedures such as ECG, phlebotomy, spirometry, vital signs, cannulation
• Record data in CRFs and report adverse events to investigators
• Cooperate with study monitors and participate in daily huddles

Skills

Clinical research

GCP knowledge

Nursing license

MS Windows

MS Office

Communication skills

Organizational skills

Attention to detail

Teamwork

Education

Bachelor's degree in Nursing

Tools

MS Windows

MS Office

Job description

Orion Group Life Sciences are currently recruiting a Research Nurse on behalf of our Multinational Biopharmaceutical Client based in York on an initial 6-Month contract with potential to extend.

• 24 hours per week, typically spread over 3 full days on site at a GP practice in York, with flexibility in the specific days but restricted to weekdays.

PURPOSE

Support study sites in the coordination of Phase I-IV clinical research studies, ensuring that studies are carried out according to protocol, standard operating procedures, GCP, and other applicable guidelines and regulations.

RESPONSIBILITIES

• Coordinate clinical research studies conducted by a supervising principle investigator.
• Update and maintain skills, training and knowledge of current best nursing practice and topics related to clinical research.
• Safeguard the well-being of the subjects and ensure and maintain high standards:
  • Maintain a safe environment in accordance with the Health and Safety policies;
  • Act as volunteer advocate;
  • Deal with volunteer and visitor concerns in a pro-active manner and taking remedial action as required;
  • Assist staff, both registered and unregistered in Nursing Practices and the delivery of care to the volunteer;
  • Report any deviation from normal practice to senior staff.
• Support study conducts by:
  • Review of the study protocol, case report form (CRF), other study documents, and electronic data capture systems;
  • Participate in project meetings with the project team as needed;
  • Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, setting up equipment and documents;
  • Plan logistical activity for procedures as per protocol;
  • Generate volunteer instructions;
  • Identify and obtain required supplies and equipment;
  • Prepare and deliver study specific training materials, documents, and records;
  • Troubleshoot study issues;
  • Participate in huddles to ensure daily tasks are assigned to team members are executed to the expected standards;
  • Assist with data quality checking and query resolution to ensure that data collected on study volunteers adhere to study protocol and ensuring quality control for content accuracy and completeness.
• Recruit and Screen volunteers for inclusion in study based on pre-determined criteria.
• Orientate volunteers to the study and the site including the purpose of the study, procedures and practical issues such as timelines for visits.
• Responsible for the correct administration and custody of study drug according to site standard operating procedures.
• Perform a variety of complex clinical procedures on subjects including but not limited to ECG, sample collection including phlebotomy, spirometry, vital signs, cannulation, and cardiac telemetry monitoring.
• Collect, record, and report clinical data and findings appropriately in case report forms (CRFs). Collaborate closely with study investigator informing on relevant adverse events and serious adverse events according to procedures outlined in the protocol.
• Cooperate with study monitor and reserve sufficient time for questions during monitoring.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Good knowledge of clinical trials
• In-depth knowledge of the principles of Good Clinical Practices (GCP)
• Good skill in using MS Windows and Office applications
• Effective written and verbal communication skills including good command of the English language
• Excellent interpersonal skills
• Excellent problem-solving skills
• Effective organizational skills
• Ability to pay close attention to detail
• Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

• Bachelor's degree or educational equivalent in Nursing and 1-year relevant experience; or equivalent combination of education, training and experience
• Current active nursing license in the state, country, or region in which the site resides
• Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies

PHYSICAL REQUIREMENTS

• Use of telephone and face-to-face communication requiring accurate perception of speech
• Use of keyboard requiring repetitive motion of fingers
• Frequent mobilization around the facility

People are our business worldwide

Orion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services - Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management - across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.