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School of Nursing

Scientific Officer (Temporary Appointment)

(Ref. 250611012)

[Appointment period: twelve months initially, with the possibility of further appointment]

Duties 

The appointee will play a crucial role in supporting the implementation and management of clinical trials within the Faculty of Health and Social Sciences Clinical Trials Unit.  This position involves collaboration with researchers, clinicians, and other stakeholders to ensure the scientific integrity and success of clinical research projects.  He/She will be required to: 

(a)    offer expert advice on study design, statistical analysis, and epidemiological methodologies to staff and collaborators; 

(b)    provide training and support to staff and collaborators on clinical trial processes, data management and regulatory compliance; 

(c)    serve as the primary point of contact for external consultants, facilitating communication and collaboration to ensure alignment with clinical trial objectives and timelines;

(d)    work closely with the management team to develop strategic plans, optimise trial processes, and ensure the efficient execution of clinical research projects; 

(e)    coordinate activities between internal teams and external consultants to ensure seamless integration of expertise and resources; 

(f)    contribute to the development of long-term strategies for the Clinical Trials Unit and identify opportunities for improvement and growth;

(g)    prepare comprehensive reports and documentation to communicate trial progress and outcomes to the management team and external stakeholders; and 

(h)    perform any other duties as assigned by the Head of Unit or his/her delegates.

Qualifications 

Applicants should: 

(a)    have a Master’s degree or above in Public Health, Epidemiology, Biostatistics or a related discipline;

(b)    have at least five years of relevant experience, preferably in clinical trial design, management, and analysis in a clinical trials unit or similar research environment; 

(c)    have a strong understanding of regulatory requirements and ethical guidelines for clinical research;

(d)    have proficiency in statistical software and data management tools;

(e)    have excellent communication and interpersonal skills;

(f)    have strong organisational and problem-solving abilities; and

(g)    be able to work independently and be a good team player.

Preference will be given to those who have a strong understanding of Good Clinical Practice (GCP).

Conditions of Service

A highly competitive remuneration package will be offered. 


Consideration of applications will commence on 25 June 2025 until the position is filled.



Posting date: 11 June 2025