Clinical Research Associate
5 days ago
We are seeking an experienced Clinical Research Associate to join our team as a key member in managing oncology trials. The ideal candidate will have a strong background in clinical research, excellent communication skills, and the ability to work independently.
Job Responsibilities:- Monitor multiple oncology trials, ensuring compliance with Good Clinical Practice (GCP) guidelines and local regulations.
- Develop site startup documents, including SIV agendas, and provide quality control reviews of study documents.
- Act as a lead Site Manager, training other SMs on studies and mentoring junior team members.
- Represent Local Trial Managers or Site Managers on Study Management Teams (SMTs) and meetings.
To be successful in this role, you will need:
- A minimum of a B.Sc., R.N., or equivalent degree in Biological Sciences.
- A minimum of 2 years' experience in monitoring pharmaceutical industry clinical trials, preferably in oncology.
- An analytical/risk-based monitoring experience is an asset.
- Strong communication and influencing skills to effectively manage study sites remotely and face-to-face.
- Ability to operate and use various systems and databases, such as CTMS, EDC, eTMF, IWRS, and safety reporting.
- Familiarity with ICH guidelines and local regulatory requirements.
In addition to your competitive salary, we offer a range of benefits to support your well-being and work-life balance. These include:
- Varying annual leave entitlements.
- A range of health insurance options to suit your needs.
- Competitive retirement planning offerings.
- A Global Employee Assistance Programme for mental health support.
We are committed to providing an inclusive and accessible environment for all candidates and employees. Our company values diversity, equity, and inclusion, and we strive to create a workplace where everyone can thrive.
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Clinical Research Associate
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Clinical Research Associate
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