Careers
Recognised internationally as the Australian CRO of choice, Trident Clinical Research is at the forefront of the clinical research industry. With offices in all major Australian cities, New Zealand and Mumbai, India, we are renowned as an innovative employer, with flexible working conditions, a professional working environment, and excellent benefits.
Employment Opportunities
Clinical Research Associate/Senior Clinical Research Associate – Sydney, Adelaide and Auckland
At Trident Clinical Research we are well known for our flexible working environment, supportive culture, experienced staff and professionalism. With a growing pipeline of studies, in a number of different phases and therapeutic areas, we need to expand and are looking for new staff to join our team.
Trident is looking for an experienced CRA or SCRA to join the Sydney, Adelaide and Auckland teams.
You need to be a motivated and proactive individual who has exceptional communication and organisational skills.
Requirements:
- At least 1 year monitoring experience with a pharmaceutical company or CRO with demonstrated relevant competencies with respect to a diverse range of clinical research activities;
- A thorough knowledge of ICH Guidelines for Good Clinical Practice and relevant local requirements.
- A tertiary qualification in pharmacy, biological sciences, and/or tertiary qualified or a registered nurse.
Overview:
These are full-time, permanent office based positions based in our offices located in Gordon (Sydney), Port Adelaide (Adelaide) and Mairangi Bay (Auckland). Part-time (3 days/week) applicants will also be considered.
Senior Quality Assurance Associate
We are seeking an experienced Clinical Quality
Assurance professional.
Applicants for the Senior Quality Assurance
Associate position should possess the following:
- Tertiary qualification in pharmacy, life/health related sciences, tertiary qualified or registered nurse and /or an appropriate
Quality qualification.
- Experience in auditing Phase I - III
clinical trials.
- Extensive experience in maintaining a
company quality framework in Pharma or a
CRO thorough knowledge of ICH, NHMRC,
FDA and TGA regulations and requirements.
- Excellent attention to detail, report writing
and English skills and computer literacy.
The Senior QA Associate is office based preferably in Adelaide but Sydney and Melbourne candidates will be considered.
All applications will be treated in strictest confidence. If you are interested, please send your CV and cover letter to recruitment@tridentclinicalresearch.com, referencing the position you are applying for. Position descriptions will not be provided.
ENQUIRIES
Adelaide Office (Head Office)
Tel: +61-8-8447 3500
Fax: +61-8-8447 3511
