2d ago

Clinical Research Associate - MEA unblinded role

Covance

Save this job
Save job
Unlock your match score
Similar jobs pay
$90k - $100k
Work type
Full Time
Contract type
Permanent
How this job matches you
% match
Get your match score for free
Pay guide
Market insights based on all Clinical Research jobs in Sydney NSW
Similar jobs pay range
$90k - $100k
Market average
$100k
$38k - $66k
7 jobs
$66k - $94k
90 jobs
$94k - $122k
287 jobs
$122k - $150k
10 jobs
$150k - $250k+
15 jobs
$100k
Market average
$60k
$250k+
Actual pay is not disclosed by the employer
Skills
CLINICAL RESEARCH
CRA
DATA MANAGEMENT
GCP
ICH
MARKETING ANALYSIS
MEDICAL/CLINICAL
PHARMACEUTICAL LABORATORY
SITE MONITORING
WRITTEN AND VERBAL

Full job description

CRA I - MEA is an essential member of a Clinical Project Team responsible for the
execution of a Clinical Research Project.

The degree of responsibility given to the CRA I - MEA shall reflect their experience, and level of contribution which they can make to the project. The work will involve Operations activities which will be conducted for designated projects as well as some travel to conduct site visits or to attend client or internal team meetings as needed. The CRA I - MEA will be responsible for assisting with ensuring quality and integrity of data, and additional study related activities to support the efforts of study team members. Activities will be conducted in compliance with Company or Sponsor SOPs, regulatory standards and applicable.

You may be office based if you live in Melbourne.
If you are Brisbane based you should have some prior monitoring experience, ideally at least three to six months. You may have to opportunity to be fully home based, with occasional travel to hospital sites expected.
Minimum Required:
♦ External Candidates
o University or college degree, or certification in a related allied health profession from
an appropriately accredited institution (e.g., nursing licensure)
AND
o A minimum of 2 years of experience in a related role (e.g. site management, in-house
CRA, study coordinator, research nurse, etc.)
♦ Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory
requirements
♦ Basic understanding of the clinical trial process
♦ Valid Driver’s License
Preferred:
♦ Working knowledge of Covance SOPs for site monitoring
Minimum Required:
o University or college degree, or certification in a related allied health profession
from an appropriately accredited institution (e.g., nursing licensure)
AND
o a minimum of 2 years e of industry experience in a related role (e.g. site management,
in-house CRA, study coordinator, research nurse, etc.)
♦ Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH
Guidelines and GCP
♦ Ability to work within a project team
♦ Good planning, organization and problem solving abilities
♦ Good communication skills, oral and written
♦ Good computer skills
♦ Works efficiently and effectively in a matrix environment
♦ Fluent in local office language and in English, both written and verbal
Draft: Dec 2020 Page 6 of 7
Preferred:
♦ One (1) or more additional years of experience in a related field (i.e., medical, clinical,
pharmaceutical laboratory, research, data analysis, data management or technical writing) is
preferred.

Job details
Date posted
16 Sep 2021
Category
Science, Technology & Environment
Occupation
Clinical Research
Similar jobs pay
$90k - $100k
Contract type
Permanent
Work type
Full Time
Job mode
Standard hours
Work Authorisation
Australian Citizen / Permanent Resident

You may also be interested in these jobs