In-Demand clinical research associate (level i/ii) Jobs in greater adelaide sa

Clinical Research Associate (Level I/II)
Thermo Fisher Scientific —Greater Adelaide SA
- Full-time
- Laboratory
- Patient monitoring
- Microsoft Office
- Parental leave
- Employee assistance program
Clinical Research Assistant - Research - Clinical
Advara HeartCare —Greater Adelaide SA
- Full-time
- Laboratory experience
- Research
- Microsoft Office
2d
Clinical Research Assistant
Icon Group —Greater Adelaide SA
- Full-time
- Nursing
- Research
- Microsoft Office
4d
CRA II- SCRA I
サイネオス・ヘルス —Greater Adelaide SA
- Contract
- Remote
- Patient monitoring
- Bachelor's degree
- Patient care
Sr CRA I/ II (0.6 FTE) Melbourne/ Sydney
サイネオス・ヘルス —Greater Adelaide SA
- Contract
- Patient monitoring
- Bachelor's degree
- Patient care
CRA I, Australia (no monitoring experience required)
サイネオス・ヘルス —Greater Adelaide SA
- Contract
- Remote
- Patient monitoring
- Bachelor's degree
- Computer skills
5d
CRA I, Sydney or Melbourne (no monitoring experience required)
サイネオス・ヘルス —Greater Adelaide SA
- Contract
- Remote
- Patient monitoring
- Bachelor's degree
- Computer skills
5d
Clinical Trials Centre Officer
SA Health —Adelaide SA
- $71,589 - $76,033 a year
- Full-time
- Microsoft Office
- Annual leave
- Employee assistance program
12d
Medical Oncology Clinical Research Fellow 2027 - CALHN
SA Health —Adelaide SA
- $99,707 - $169,648 a year
- Full-time
- Medicine
- Health insurance
- Employee assistance program
6d
CRA II- SCRA (Melb/ Sydney)
サイネオス・ヘルス —Greater Adelaide SA
- Contract
- Remote
- Patient monitoring
- Bachelor's degree
- Patient care
Cardiology Research Senior Co-ordinator and Clinical Nurse
SA Health —Adelaide SA
- $90,913 - $114,917 a year
- Part-time
- Annual leave
- Employee assistance program
4d
Lecturer / Associate Lecturer in Law
Flinders University —Bedford Park SA
- $90,930 - $137,122 a year
- Full-time
- Doctoral degree
- University
- Teaching
6d
Postdoctoral Research Associate/Research Fellow
Flinders University —Bedford Park SA
- $90,930 - $137,122 a year
- Full-time
- Doctoral degree
- Data analysis skills
- Laboratory experience
SCRA I
サイネオス・ヘルス —Greater Adelaide SA
- Contract
- Patient monitoring
- Bachelor's degree
- Patient care
5d
Sr. CRA (Level II)
Thermo Fisher Scientific —Greater Adelaide SA
- Full-time
- Laboratory
- Microsoft Excel
- Patient monitoring
- Parental leave
- Employee assistance program
Territory Manager - Medical Devices
BD —Greater Adelaide SA
- Communication skills
- Hospital experience
Associate Nurse Unit Manager - Karra Rehab Unit- TQEH
SA Health —Greater Adelaide SA
- $107,487 - $114,917 a year
- Full-time
- Nursing
- Annual leave
- Employee assistance program
11d
Associate Nurse Unit Manager - Perioperative Recovery (Zone 4/5)
SA Health —Adelaide SA
- $107,487 - $114,917 a year
- Part-time
- Annual leave
- Employee assistance program
3d
Associate Nurse Unit Manager South East
SA Health —Greater Adelaide SA
- $107,487 - $114,917 a year
- Full-time
- Annual leave
- Employee assistance program

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Clinical Research Associate (Level I/II)

Thermo Fisher Scientific -
Greater Adelaide SA

Apply Now

Job Details

Full-time

Benefits

Birthday leave
Parental leave
Employee assistance program
Paid volunteer leave

Qualifications

Patient monitoring
Microsoft Office
Education
Presentation skills
Bachelor's degree
Driver Licence
Medical terminology
Communication skills
Time management

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate (Level I/II) – Make an Impact at the Forefront of Innovation.

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level I/ II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Conducts risk-based site monitoring (on-site and remote), ensuring protocol compliance, data accuracy (SDR/SDV/CRF), and investigational product accountability; identifies issues using root cause analysis and drives corrective/preventive actions through to resolution.
Manages site lifecycle activities including feasibility, initiation, routine monitoring, and close-out, ensuring adherence to ICH-GCP, regulatory requirements, and study protocols.
Maintains complete and accurate trial documentation and systems (e.g. CTMS), provides status updates to the clinical team, and supports investigator payments where required.
Acts as the key liaison between sites, sponsor, and project team; escalates and resolves issues, supports audits/inspections, and ensures ongoing site communication and performance.
Contributes to team deliverables and continuous improvement initiatives, while completing administrative tasks in a timely manner.

Education and Experience Requirements:

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
Valid Australian driver's license
Australian Citizenship or Permanent Resident required

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Proven clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manage Risk Based Monitoring concepts and processes
Good oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Good organizational and time management skills
Effective interpersonal skills
Attention to detail
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions

Benefits

Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer.

Health & Wellbeing: Join a company that prioritizes your health & wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues.
Flexibility: Balance your work and personal life with flexible arrangements.
Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave.
Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you.
Learning & Development: Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.

Thermo Fisher Scientific Australia WGEA Employer of Choice for Gender Equality

Apply Now

Refine Your Search

clinical research associate (level i/ii) jobs in greater adelaide sa

Clinical Research Associate (Level I/II)

Clinical Research Assistant - Research - Clinical

Clinical Research Assistant

CRA II- SCRA I

Sr CRA I/ II (0.6 FTE) Melbourne/ Sydney

CRA I, Australia (no monitoring experience required)

CRA I, Sydney or Melbourne (no monitoring experience required)

Clinical Trials Centre Officer

Medical Oncology Clinical Research Fellow 2027 - CALHN

CRA II- SCRA (Melb/ Sydney)

Cardiology Research Senior Co-ordinator and Clinical Nurse

Lecturer / Associate Lecturer in Law

Postdoctoral Research Associate/Research Fellow

SCRA I

Sr. CRA (Level II)

Territory Manager - Medical Devices

Associate Nurse Unit Manager - Karra Rehab Unit- TQEH

Associate Nurse Unit Manager - Perioperative Recovery (Zone 4/5)

Associate Nurse Unit Manager South East

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