About the Role:
* As a Clinical Research Associate, you will be responsible for conducting site qualification, interim monitoring and study closeout visits.
* You will conduct all clinical site activities according to the monitoring plan and in accordance with the study timelines.
* You will act as a central point of contact at investigator meetings and site initiation visits.
* You will manage all aspects of the clinical monitoring process.
* You will build and develop relationships with site stakeholders.
* You will identify, evaluate and recommend new potential investigators and sites on an ongoing basis.
* You will mentor junior Clinical Research Associates.
To be successful in this role, you will require:
* A minimum of 5 years experience in clinical research and 2 years of independent monitoring experience or a minimum of 1 year of independent monitoring experience for a more senior position.
* A solid understanding and knowledge of appropriate therapeutic indications as they relate to the conduct of clinical trials.
* A sound knowledge and understanding of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
* Strong planning and organisational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.
* Exceptional communication skills as well as strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity.
* Demonstrated business ethics and integrity.
* Appropriate tertiary qualifications in the medical, pharmaceutical or healthcare disciplines.
We Offer:
* An attractive remuneration package.
* Genuine work-life balance.
* Flexibility and career stability and security.
* Office located in a convenient location with under cover parking provided.
* Additional benefits including STAR day - one extra day off per year for you to recharge.