Clinical Research Associate II

1 day ago


Melbourne, Victoria, Australia beBeeClinicalResearch Full time $100,000 - $120,000

Clinical Research Associate II: A Critical Role in Ensuring Trial Success

In the ever-evolving landscape of clinical research, the role of a Clinical Research Associate II (CRA II) plays a pivotal part in ensuring the success of trials.

At Syneos Health, we recognize the importance of this position and are dedicated to providing our CRA IIs with the necessary tools and support to excel in their roles.

As a CRA II, you will be responsible for conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices. This includes reviewing study protocols, case report forms, and regulatory documents.

You will also develop tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and standard operating procedures.

In addition, you will contribute to the design, implementation, and delivery of processes, programs, and policies by providing expert input and feedback during development and review stages.

Your expertise will be invaluable in directing the work of lower-level professionals or managing processes and programs, including training and mentoring junior staff and overseeing their monitoring activities.

To be successful in this role, you must ensure trials are conducted in accordance with regulatory requirements and company standards by performing regular audits and inspections, and addressing any compliance issues that arise.

You will also provide guidance and support to clinical research teams, including answering questions, resolving issues, and facilitating communication between team members and stakeholders.

Ultimately, your goal will be to maintain accurate and timely documentation of monitoring activities, including writing detailed monitoring reports, tracking study progress, and updating databases.

If you are a detail-oriented individual with strong analytical and problem-solving skills, and excellent communication and interpersonal skills, we encourage you to apply for this exciting opportunity.

Requirements:

* Bachelor's degree in a related field

* Minimum of 5 years of experience in clinical research monitoring; this role is a progression within the level from a Sr CRA I

* In-depth knowledge of clinical trial processes and regulations

* Strong analytical and problem-solving skills

* Excellent communication and interpersonal skills

* Ability to work independently and as part of a team

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