Clinical Research Associate
- Company
- mexec
- Location
- Melbourne
- Salary
- Competitive
- Posted
- 21 Sep 2020
- Closes
- 19 Oct 2020
- Ref
- 3613441
- Discipline
- Clinical Research
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Clinical Research Associate
21/9/2020
The Company
Do you want to have the right balance? Do you want to work in a team that values training and success and actually takes pride in progressing their staff?
Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas and active in over 45 companies globally. Due to continual growth they are seeking a full time CRA to join their operations.
Our client has a culture of expertise that empowers teams to support their business partners.
Their values are high, and recognition and advancement are incremental to their success. Their team is stable and long term and their employees valued. Just a few reasons why mexec careers choose to represent them.
The Role
Due to continual growth they are seeking a full time CRA to join their team.
- Healthcare & Medicine
- Clinical / Medical Research
- Melbourne
- Permanent / Full Time
21/9/2020
- New opportunity due to growth
- Comprehensive training program
- Stable workforce & valued staff
The Company
Do you want to have the right balance? Do you want to work in a team that values training and success and actually takes pride in progressing their staff?
Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas and active in over 45 companies globally. Due to continual growth they are seeking a full time CRA to join their operations.
Our client has a culture of expertise that empowers teams to support their business partners.
Their values are high, and recognition and advancement are incremental to their success. Their team is stable and long term and their employees valued. Just a few reasons why mexec careers choose to represent them.
The Role
Due to continual growth they are seeking a full time CRA to join their team.
- Verify that the rights and well-being of subjects are protected, the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial is in compliance with the currently approved protocol/amendment(s), GCP, and applicable regulatory requirement(s);
- Ensure site compliance while conducting qualification, study initiation, routine monitoring, and study site close-out visits for research sites according to our clients/Sponsor Standard Operating Procedures (SOPs);
- Serve as the primary resource to the clinical investigator and site staff;
- Maintain close collaboration, interaction, and effective working relationships with our clients internal cross-functional teams;
- Ensure quality completion of visit reports, follow-up letters, and maintenance of study-related databases and their internal Monitoring Portal; and
- Must have and maintain a valid driver’s license and the ability to drive to monitoring sites.
- Bachelor's degree with at least 2-5 years of Experience as a Clinical Research Associate;
- Approximately 60-80% non-local, national travel is required;
- Must have a minimum of a bachelor’s degree in a health or science related field;
- Proficient knowledge of Microsoft® Office;
- Outstanding communication skills; and
- Must be detail-oriented and efficient in time management
- Demonstrated ability to independently function as a Lead CRA (on more complex studies as applicable), including the ability to effectively plan, delegate, and review the work of others;
- Demonstrated ability to present at meetings, including the ability to seek, make, and develop suggestions;
- Knowledgeable enough about Clinical Monitoring practices and procedures to represent the function in internal and external (e.g., business development) meetings.