Clinical Research Nurse (CRN)

Job Description

Title: Clinical Research Nurse (CRN)

Company Name: Toxicology Society of Bangladesh (TSB)

Vacancy: --

Age: 22 to 40 years

Job Location: Chattogram, Rajshahi (Rajshahi Sadar)

Salary: Negotiable

Experience:

• 1 to 2 years
• The applicants should have experience in the following business area(s): Hospital, Research Organization
• Freshers are also encouraged to apply.

• Bachelor of Science (BSc)
• Diploma in Nursing

• 1 to 2 years
• The applicants should have experience in the following business area(s): Hospital, Research Organization
• Freshers are also encouraged to apply.

• Age 22 to 40 years

• 1 to 2 years(s) of Clinical trial experience is preferred
• The applicants should have experience in the following areas: Research Nurse
• The applicants should have experience in the following business area(s): Research Organization

Key Skills & Competencies:

• Experience in international clinical research projects will be preferred
• Critical thinking and problem-solving skills
• Quick learner & ability to assume responsibility
• Technology Proficiency
• Demonstrated ability to multi-task and prioritize in a fast-paced environment
• Effective communication and Interpersonal skills
• Competence in conducting health assessments
• Sensitivity to cultural differences and the ability to work with diverse populations
• High level of work ethic and detail oriented
• Excellent coordination and organizational skills.
• Teamwork
• Knowledge of Good Clinical Practice (GCP).
• Flexibility in work hours to accommodate study timeline, patient recruitment and potential urgent requests.

Job Purpose:

This position will provide clinical support to the clinical study team for the proper conduction of Clinical studies at the site as per the study protocol, regulatory guidelines & ICH-GCP. Under the supervision of the research assistants, He / She is responsible for the proper medical care of the study participants. He / She will be conducting the study following the protocol with adequate compliance. The CRN is also obligated to ensure the project is conducted in compliance with the applicable laws and regulations to ensure the well-being of the participants.

Key Stakeholders:

Principle Investigator/ Co-investigator

Other critical stakeholders:

Clinical research assistant, Site Trial coordinator, Junior Trial Manager, Senior Trial Manager, Research administrator & logistics manager, Trial Data Associate

Key Performance Indicators:

Participant Recruitment and Retention, Study Protocol Adherence, Sample collection, Data Entry, Patient safety & Care, Timeliness of CRF Completion, Stakeholder Collaboration

Key Responsibilities:

• Conduct preliminary health assessments of the participants to decide eligibility for participation in the trial.

• Explain the trial procedures, potential risks, and benefits to participants.

• Collect and record accurate medical histories and demographic information.

• Assist Clinical Research Associates (CRAs) in ensuring the proper completion of case report forms (CRFs) and other required documentation.

• Administer medications to patients, as directed by Clinical Research Associates (CRAs), in accordance with the study protocol and established guidelines.

• Monitor participants for adverse reactions and provide appropriate care as needed, following instructions from the Clinical Research Associate (CRA) and adhering to study protocol and established guidelines.

• Support the CRA for blood sample collections from the research participants, processing and storage of it as per the study protocol.

• Assist Clinical Research Associates (CRAs) when performing the POC formate assays and laboratory formate assays.If required, educate participants on post-administration care and potential side effects.

• Report any adverse events or deviations from the protocol to the study coordinator or principal investigator.

• Participate in regular internal team meetings to discuss progress, challenges, and potential improvements.

• Ensure proper storage and handling of medications.

• Provide support to the clinical research team, when required, in preparing and packaging samples for transfer according to the study protocol.

• Support Study monitoring or audit when required.

• Perform other job-related duties as required.