Senior Clinical Research Associate - NSW

Novotech Global; Sydney; Ibrido; AUD 85.000 - 125.000; Tempo pieno

Descrizione del lavoro

Novotech Global is seeking a Clinical Research Associate (CRA) to safeguard trial participant rights and ensure data quality across source documents. The CRA serves as the primary contact between Investigational Sites, Novotech and Sponsors, overseeing site relationships and adherence to ICH GCP and SOPs.

Based in Sydney with hybrid working arrangements and flexible hours, this role requires strong time management, teamwork, and attention to detail to support timely trial delivery and regulatory

Competenze

• Graduate in clinical or life sciences-related field.
• Experience in research or pharmaceutical industry preferred.
• Unrestricted working rights in Australia; visa sponsorship not available.
• Strong time management, attention to detail, teamwork and computer literacy.

Mansioni

• Build relationships with Principal Investigators, study coordinators, pharmacists and site personnel to ensure efficient management of trials.
• Foster internal and external customer relationships to ensure timely project delivery per study requirements.
• Collaborate with IHCRA and RSA, prepare site essential documents and support ethics/regulatory submission processes as needed.
• Understand local and international regulatory requirements relevant to specific trials.
• Ensure recruitment of participants per site targets and support recruitment planning.
• Monitor investigational sites across all ICH GCP monitoring visit types (Site Selection, Initiation, Monitoring, Close Out).

Conoscenze

Time management

Attention to detail

Teamwork

Computer literacy

Formazione

Graduate in clinical or life sciences

Descrizione del lavoro

The Clinical Research Associate (CRA), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs.

This role will be based in Sydney and we offer hybrid working arrangements and full flexibility in working hours to ensure our staff achieve the work-life balance often missing in this role.

Minimum Qualifications & Experience

Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. For our current opportunities we require experience of working in the research, pharmaceutical industry or a related field per job level as follows:

• SCRA: minimum of 3 years of CRA independent monitoring experience, preferably within Oncology

You must have full unrestricted working rights in Australia to be considered for this role . We unfortunately cannot provide sponsorship for this role.

Responsibilities:

• CRAs primary responsibility is to build relationships with Principal Investigators, study coordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited and smooth management of clinical trials.
• Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines.
• collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed.
• In collaboration with Regulatory Start-up (RSU) Team, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials.
• Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required.
• Monitoring of investigational sites as per ICH GCP This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblended pharmacy visits, and co-monitoring visits.