Senior Clinical Research Associate

Clinipace; Brisbane; On-site; AUD 90,000 - 120,000; Full time

Job summary

Clinipace in Brisbane is seeking a Senior Clinical Research Associate to monitor investigational sites and ensure subject safety while delivering high-quality data in line with GCP/ICH, ISO14155, and sponsor SOPs.

You will build strong site relationships, serve as liaison between Sponsor and sites, and oversee visits from pre-study to close-out, ensuring regulatory documentation is complete and deadlines are met.

Qualifications

• Requires a 4-year college degree or equivalent clinical research experience.
• Minimum 3 years on-site monitoring in clinical studies.
• Experience across multiple indications and study types.
• Strong written and verbal communication skills.
• Proficiency in English and local language.

Responsibilities

• Serves as primary contact for assigned sites.
• Verifies that investigator, staff, and site facilities remain adequate.
• Schedules and conducts pre-study, initiation, interim, and close-out visits per Monitoring Plan.
• Ensures studies are conducted per protocol and applicable regulations.
• Verifies informed consent is obtained for all subjects.
• Performs SDV against CRF/EDC entries with proper documentation.
• Manages product accountability, storage, and inventory where applicable.
• Reports adverse events per regulatory requirements and Monitoring Plan.
• Maintains site regulatory binder completeness and documentation.
• Supports translations of essential documents and regulatory submissions if needed.
• Provides mentorship and training to junior CRAs as required.

Skills

On-site monitoring

GCP/ICH knowledge

Excellent communication

English proficiency

Education

4-year college degree

Alternative 3+ years clinical research experience

Job description

Job Title: Senior Clinical Research Associate

Job Location: Brisbane

Job Overview:

The Senior Clinical Research Associate I monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines, ISO14155, and other applicable regulations. Builds, manages and supports strong site relationships while serving as liaison between the Sponsor and assigned sites.

Job Duties and Responsibilities:

• Provides support to Project Team and Clinical Operations Team.
• Maintains strong working knowledge of protocols and Monitoring Plans for assigned projects.
• Demonstrates strong written and verbal communication skills.
• Serves as primary contact for assigned research sites.
• Verifies that the investigator, staff, and site facilities remain adequate throughout the trial period.
• Responsible for the scheduling and conduct of pre-study visits, initiation visits, interim monitoring visits and close-out visits according to the Monitoring Plan.
• Ensures research sites conduct studies according to protocol requirements or investigational plan and applicable regulations and guidelines.
• Verifies the rights and well-being of trial subjects are protected.
• Reconciles site regulatory binder assuring collection and completeness of regulatory documents.
• Collects and ensures completeness of all essential regulatory documentation from sites from study start-up through close-out.
• May support translations of essential documents.
• May support submission of trials to IRB/IEC and regulatory authorities.
• Verifies that written informed consent was obtained before each subject’s participation in the trial.
• Verifies that the investigator is enrolling only eligible subjects.
• Performs source data verification against Case Report Form/Electronic Data Capture entries in compliance with the Monitoring Plan. Ensures accurate and complete data and that corrections are appropriately documented by authorized site staff.
• Verifies the quality of all recorded data. Issues and ensures timely resolution of all data queries remotely or at investigator site.
• Performs Investigational Product accountability, including product storage, inventory, return/destruction, and dispensing/receipt records.
• Verifies and supports the recording and reporting of adverse events/serious adverse events. Ensures all types of adverse events are reported and tracked per regulatory requirements and the Monitoring Plan.
• Ensures that sites have sufficient project specific supplies.
• Manages investigative sites in respect to the trial conduct and motivates sites to meet study goals.
• Communicates deviations from the protocol, SOPs, and/or GCP, to the investigator, and project management team and takes appropriate action to prevent recurrence.
• Delivers high quality written trip reports, confirmation and follow-up letters within timelines of SOPs and monitoring plans.
• Participates in site audits, as requested.
• May conduct site and study feasibility assessments.
• Provides input into study documentation and monitoring worksheets.
• Uphold the confidentiality agreements with all clients and colleagues outside Caidya Clinical Research.
• Pays attention to signals of fraud, misconduct and escalates per Caidya SOP.
• Work according to the Caidya Quality Management System and actively participate in giving feedback and suggesting improvements to current processes.
• Work according to the project-specific timelines and budget agreement, which has been agreed upon with the sponsor. Accurately document the time spent per project in the Caidya time allocation system.
• May conduct Team calls and Sponsor calls (as needed).
• May provide project-specific performance feedback.
• May serve as site contact for protocol clarifications and subject enrollment.
• May manage Protocol Deviation documentation, tracking, and escalation.
• May relate project status and issues to Project Manager and/or CRAs.
• May serve as Sponsor contact for monitoring/site issues.
• Attends and participates in team teleconferences/meetings providing mentoring and training.
• Participates in relevant trial meetings, e.g. Kick-off, Investigator, and Monitor meetings, and provides support, as requested.
• Demonstrates flexibility and adaptability.
• Assists project team in development of monitoring guidelines and tools.
• Proactively identifies, manages, escalates (as needed) and resolves site issues effectively and independently.
• Provides mentorship, training and direction to Clinical Research Associates when needed.
• May conduct SOV and QAV assessments

Supervisory Responsibilities:

No supervisory responsibilities.

Job Requirements:

• Education
  • 4-year college graduate, preferably with a healthcare or life science degree.
  • In lieu of a degree, candidates with 3 or more years of relevant clinical research experience in pharmaceutical or CRO industries will be considered.
• Experience
  • Minimum of 3 years of experience in on-site monitoring of clinical studies
  • Monitoring experiences in several different indications and study types
  • Experience in all areas of monitoring (on-site, remote, etc.)
• Strong written and verbal communication skills
• Strong interpersonal skills
• Expert monitoring skills to independently conduct all types of site monitoring visits
• Good documentation skills; good command of English and the local language in the area of activity (reading, writing, understanding)
• Comprehensive knowledge of GCP/ICH guidelines
• Proficiency in medical terminology
• Able to exercise judgment within defined procedures and practices and to determine appropriate action independently.
• Strong problem-solving skills
• Ability to work in a matrix environment
• Strong time management and organizational skills
• Capabilities
  • Ability to drive an automobile and have a valid driver’s license, if applicable.
  • Valid passport required in the case of international business travel.
  • Ability to travel up to 80%.