Life Sciences WA Jobs in Australia

Job Description · A global clinical research organization seeks an Inhouse Clinical Research Associate to support the clinical team with project-specific tasks. · Manage clinical study documentation · Evaluate compliance with ICH GCP guidelines · Maintain the Clinical Trial Manag ...

A renowned clinical research organization is seeking a Clinical Research Associate (CRAII - CRAIII) to manage site relationships. · Key Responsibilities: · Ensure compliance with regulatory standards · The ideal candidate will have a graduate degree in clinical or life sciences a ...

Job Summary · The Proposal Budget And Contracts Associate develops high-quality proposals, budgets, and contracts. · ...

Job Description: · Manage clinical study documentation · E nsure compliance with ICH GCP · This hybrid role requires a commitment to working in the office at least 2 days a week. · Candidates should have at least 1 year of relevant experience and knowledge in Life Sciences. · ...

A clinical research organization in Australia seeks a Clinical Research Associate with graduate degree in clinical or life sciences. · Responsibilities: · Manage site relationships · Ensure compliance with regulatory standards · ...

Developing proposals requires generating high-quality documents within tight timelines. The Proposal, Budget and Contracts Associate ensures timely delivery of budgets and contracts by researching statistics and company information. · Prepare proposal templates with Novotech bran ...

The Clinical Research Associate Role Summary · In this key position you will be responsible for ensuring trial participant protection, accurate data reporting and site compliance. As a member of our team you can expect hybrid work arrangements allowing flexibility in work hours. ...

Job Title: · Inhouse Clinical Research Associate · About Us: · We are Novotech , a global full service clinical Contract Research Organization (CRO) headquartered in Sydney,Australia. · ...

Responsibilities: · • Support the clinical team's in-house activities on assigned projects. · • Coordinate and maintain clinical study documentation · • Manage Trial Master Files · • Tracking documents · • Preparation for internal/external audits · • Routine QC reviews & final r ...

A leading clinical research organization seeks Clinical Research Associates to ensure trial participant wellbeing and data accuracy. · The role involves managing site relationships, · conducting clinical trials according to regulatory requirements, · demonstrating expertise in mo ...

Job Title: Clinical Research Associate · The primary responsibility is ensuring rights & wellbeing of trial participants protected. Data reported must be accurate, complete & verifiable. · Graduate degree in clinical or life sciences field · Good time management skills, attention ...