Clinical Research Associate, Cns, Rare Diseases

4 weeks ago

Sydney, Australia Worldwide Clinical Trials Full time

**Requisition Number**
**6072**

**Employment Type***:
**Regular**

Do you have a passion for mentoring the Next Generation of CRAs field monitors? Are you looking for a position where you will be groomed for a leadership role? If so, this Job Is For YOU. Feel the reward of impacting someone else's career while preparing for a leadership role in clinical trials. Our hiring manager, Patsy Recabarren, will be investing in your career growth & development.

**Who we are**

We’re a global, midsize CRO that pushes boundaries, innovates, and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

**What Clinical Operations Site Management does at Worldwide**

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience - one you can’t get anywhere else, with a team unlike anyone else.

At Worldwide we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.

**What you will do**

Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly late phase (II-III).

Conduct all types of visits - site qualifications, initiation, monitoring, site management and close out visits.

Ensure adherence and compliance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs).

Assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.

**What you will bring to the role**

Excellent interpersonal, oral, and written communication skills in English

Superior organizational skills with attention to details

Ability to work with little or no supervision

Proficiency in Microsoft Office, CTMS and EDC Systems

**Your experience**

Bachelor’s Degree or a Nursing Degree required

Experience with Phase II-III CNS and Oncology Clinical Trials

Ability to meet the travel requirements of the job. Our metrics are 6-8 days on site per month.

**Why Worldwide**

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.
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