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  environment, and excellent benefits.

We are currently searching for outstanding candidates in the following fields:

• Clinical project managers
• Clinical research associates
• Clinical data associates
• Clinical trials assistants.

Employment Opportunities

Trident Clinical Research is known in the industry for providing employees with a great worklife balance.  Due to a growing project pipeline, the company is looking for an experienced Medical Writer to be responsible for the development of a range of high quality clinical research documents (clinical study reports, protocols, investigator brochures, patient information sheets).  You will have the opportunity to work across a range of projects and therapeutic areas. 
You need to be a self-motivated and proactive individual who has exceptional communication and organisational skills with a strong attention to detail.  You need to be able to work both independently and as part of a team.  You must have at least 2 years experience in a Medical Writing role within a pharmaceutical company or CRO with a strong background in the preparation of clinical study reports to both ICH and ISO standards.  Prior experience with the development of investigator brochures and study protocols would be an advantage. You should have a thorough knowledge of ICH Guidelines for Good Clinical Practice and the ICH Guideline on Structure and Content of Clinical Study Reports, familiarity with medical device clinical trial standards (ISO 14155-1 and 14155-2) and a knowledge and understanding of scientific/medical terminology and principles.
You need to have a tertiary qualification in a scientific, medical or statistical discipline.
The position will be office based in Adelaide, Melbourne or Sydney.  Options for full-time or part-time employment will be considered. 
All applications will be treated in strictest confidence.  A position description will not be provided.  If you are interested, please send your CV and cover letter to Email: recruitment@tridentclinicalresearch.com, referencing the position you are applying for.

If you would like to be a member of our first-rate team, contact us today.

Trident Clinical Research is known in the industry for providing employees with a great worklife balance.  Due to a growing project pipeline, the company is looking for experienced CRAs and SCRAs to join the team. 

You need to be a motivated and proactive individual who has exceptional communication and organisational skills.  You must have 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.  You should have a thorough knowledge of ICH Guidelines for Good Clinical Practice and relevant local requirements.

You need to have a tertiary qualification in pharmacy, biological sciences, and/or tertiary qualified or a registered nurse.

The positions are office based, full-time, permanent positions. 

All applications will be treated in strictest confidence.  A position description will not be provided.  If you are interested, please send your CV and cover letter to Email: recruitment@tridentclinicalresearch.com, referencing the position you are applying for.

We are currently recruiting clinical data managers at our data management centre in Melbourne. We are seeking people with a broad range of skills including experience as clinical data associates, database administrators (SAS and/or Clintrial) and SAS programming in a clinical trials environment.

Our work covers a range of studies from phase I to Phase IV. We therefore require candidates who have worked in an ICH GCP compliant environment and to FDA standards. Candidates ideally will have a relevant qualification, an Australian work visa and a number of years experience in a pharmaceutical company or CRO’s data management department.