Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane
Thermo Fisher Scientific
Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane
Job Description
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionLocation: Brisbane, Australia (Home-based, 100% remote)Employment Type: Full-timeAbout the RoleAre you an experienced Clinical Research Coordinator ready to step into a Clinical Research Associate (CRA) role—or a newly appointed CRA looking to strengthen your monitoring skills? We are seeking motivated and detail-oriented professionals to join our CRA team in Queensland. This opportunity is ideal for CRCs looking to transition into monitoring, as well as junior CRAs who are early in their careers and eager to build a strong foundation.Key ResponsibilitiesPerforms and coordinates all aspects of the clinical monitoring and site management process, including but not limited to: source data review (SDR) and verification (SDV), visit reports, maintain accurate study documentation, identify & address site issues and action items.Conducts on-site and remote site visits to assess protocol and regulatory compliance and manages required documentation.Ensure trials are conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.Ensures audit readiness.Develops collaborative relationships with investigational sites.Collaborate with cross-functional teams, including Clinical Trial Managers, Study Start-Up and Regulatory teamsWhat We’re Looking ForMinimum 5+ years’ experience as a Clinical Study/Research Coordinator working on sponsor-driven trials, or an early-career Clinical Research Associate (approximately 6–12 months’ experience)Bachelor’s degree in life sciences, nursing, or a related fieldSolid understanding of clinical trial processes and ICH-GCP guidelinesStrong attention to detail, time management, and organisational skillsCritical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solvingGood oral and written communication skills, with the ability to communicate effectively with medical personnelAbility to work in a team or independently as requiredStrong computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate softwareStrong English language and grammar skillsAbility to remain flexible and adaptable in a wide range of scenariosAbility and willingness to travel extensively (approximately 70–80%)Valid Australian driver’s licence and ability to travel independently to sitesAustralian citizen or permanent resident only What We OfferStructured CRA onboarding and training program tailored to your experience levelMentorship and clear progression pathway to independent CRAExposure to a vast variety of clinical trials across different therapeutic areas and sponsorsCompetitive salary, car/travel allowance, and benefitsSupportive and collaborative team cultureWhy Join Us?We recognise the value of both strong site experience and early CRA exposure. Whether you’re stepping up from a CRC role or building on your initial CRA experience, we provide the training, support, and opportunities to help you succeed and grow your career.BenefitsJoin 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 We offer competitive remuneration, annual incentive plan bonus, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Locations
- Australia, Brisbane
Skills Required
- Microsoft Officeintermediate
Required Qualifications
- Minimum 5+ years’ experience as a Clinical Study/Research Coordinator working on sponsor-driven trials, or an early-career Clinical Research Associate (approximately 6–12 months’ experience) (experience, 5 years)
- Bachelor’s degree in life sciences, nursing, or a related field (degree in life sciences)
- Solid understanding of clinical trial processes and ICH-GCP guidelines (experience)
- Strong attention to detail, time management, and organisational skills (experience)
- Critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving (experience)
- Good oral and written communication skills, with the ability to communicate effectively with medical personnel (experience)
- Ability to work in a team or independently as required (experience)
- Strong computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software (experience)
- Strong English language and grammar skills (experience)
- Ability to remain flexible and adaptable in a wide range of scenarios (experience)
- Ability and willingness to travel extensively (approximately 70–80%) (experience)
- Valid Australian driver’s licence and ability to travel independently to sites (experience)
- Australian citizen or permanent resident only (experience)
Responsibilities
- Performs and coordinates all aspects of the clinical monitoring and site management process, including but not limited to: source data review (SDR) and verification (SDV), visit reports, maintain accurate study documentation, identify & address site issues and action items.
- Conducts on-site and remote site visits to assess protocol and regulatory compliance and manages required documentation.
- Ensure trials are conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.
- Ensures audit readiness.
- Develops collaborative relationships with investigational sites.
- Collaborate with cross-functional teams, including Clinical Trial Managers, Study Start-Up and Regulatory teams
Benefits
- general: Structured CRA onboarding and training program tailored to your experience level
- general: Mentorship and clear progression pathway to independent CRA
- general: Exposure to a vast variety of clinical trials across different therapeutic areas and sponsors
- general: Competitive salary, car/travel allowance, and benefits
- general: Supportive and collaborative team culture
- general: Why Join Us?We recognise the value of both strong site experience and early CRA exposure. Whether you’re stepping up from a CRC role or building on your initial CRA experience, we provide the training, support, and opportunities to help you succeed and grow your career.
- general: Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer.
- general: 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.
- general: 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.
- general: Flexibility: Balance your work and personal life with flexible arrangements.
- general: Flexibility: Balance your work and personal life with flexible arrangements.
- general: Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave.
- general: Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave.
- general: Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you.
- general: Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you.
- general: 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.
- general: 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.
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