Covance

Senior Clinical Research Associate I

Job Location(s) AU-Sydney | AU-Adelaide | AU-Brisbane | AU-Perth | AU-Melbourne | AU | AU-Canberra
Job Number
2020-49451
Job Category
Clinical Research Associates
Position Type
Full-Time
Telecommute
Yes

Job Overview

We are seeking an exceptional Senior Clinical Research Associate to join our extraordinary people in our clinical operations team that monitors Phase I - IV clinical trials.
 
Covance Senior Clinical Research Associates:
- Lead all aspects of study site monitoring according to Covance/Chiltern SOP, GCP, and ICH guidelines
- Partner with investigators and study coordinators on pre-study qualification and site initiation visits
- Conduct routine study site monitoring visits
- Close-out clinical sites, and ensure study files are up to date to maintain the success of the study.
 
If you are passionate about Clinical Research and a person who has experience independently monitoring Phase I - IV clinical study sites in Australia, let’s talk as we may have a job for you.
 
Covance Australia is committed to providing you the flexibility to work from home, the freedomtogrow&develop your career across all phases and areas of clinical trial operations, as well as provide state of the art technologyandprocesses that help to give you time back to enjoy family life.
 
You will join like-minded collaborative professionals at Covance who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.
 
Discover your potential in a company that truly invests in you. Talk to us to learn more and explore your career. Apply online today.
 
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Education/Qualifications

 
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
• In lieu of the above education requirement, candidates with a minimum of 6 years recent clinical monitoring experience will be considered.
• Thorough knowledge of regulatory requirements
• Thorough understanding of the drug development process
• Fluent in local office language and in English, both written and verbal
• Or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
 
 
 
 

Experience

Minimum Required:
- Two (2) years of Clinical Monitoring experience
- Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
- Advanced site monitoring skills
- Advanced study site management skills
- Advanced registry administration skills
- Ability to work with minimal supervision
- Good planning and organization skills
- Good computer skills with good working knowledge of a range of computer packages
- Advanced verbal and written communication skills
- Ability to train and supervise junior staff
- Ability to resolve project-related problems and prioritizes workload for self and team
- Ability to work within a project team
- Works efficiently and effectively in a matrix environment
- Valid Driver's License
Preferred:
- One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
- Local project coordination and/or project management experience

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