Senior Clinical Research Associate (Sr. CRA) - Oncology (Northeast)

Parexel International Corporation; Auckland; On-site; NZD 60,000 - 100,000; Full time

Job summary

An established industry player seeks a Clinical Research Associate to enhance site relationships and ensure successful trial execution. This role offers the chance to work with world-class technology and training, focusing on quality and compliance while fostering career development in clinical research. You'll engage with clinical sites, protect patient rights, and drive productivity through strategic patient recruitment. If you're looking for impact and flexibility in your career, this opportunity could be the perfect fit for you. Join a collaborative team that values growth and innovation in the clinical research field.

Benefits

Career Development Opportunities

Bonus Incentive Program

Flexible Work Environment

Remote Work Options

Qualifications

• Experience in clinical research with understanding of clinical trials.
• Ability to perform clinical monitoring activities independently.

Responsibilities

• Conduct qualification and monitoring visits at clinical sites.
• Ensure the rights and well-being of human subjects are safeguarded.
• Develop patient recruitment strategies to meet enrollment timelines.

Skills

Site Management

Clinical Trials Methodology

Interpersonal Skills

Problem-Solving Skills

Communication Skills

Computer Skills

Oncology Experience

Education

Bachelor's Degree in Biological Science

Pharmacy Degree

Tools

Clinical Trial Management System (CTMS)

Electronic Document Management System (EDMS)

MS-Office (Excel, Word)

Job description

Your time here

At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA's are accountable for using their expertise to build and maintain the site relationship and ensure they're set up for success. As the clinical sites' sole point of contact, this includes addressing and resolving site issues and questions. You'll also manage site quality and delivery from site identification through to close-out.

As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.

What you'll do

• Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
• Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
• Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
• Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
• Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
• Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

More about you

On your first day we'll expect you to have:

• Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
• Ability to perform all clinical monitoring activities independently.
• Bachelor's or equivalent degree in biological science, pharmacy or other health related discipline.
• Strong interpersonal, written, and verbal communication skills within a matrixed team.
• Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
• A client-focused approach to work and flexible attitude with respect to assignments/new learning.
• The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
• An honest and ethical work approach to promote the development of life changing treatments for patients.
• Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.
• Minimum of one year experience as a Parexel employee.
• Oncology experience required.

A little about us

Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you'll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology "super user" or collaborator are a phone call away. Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level CRA role, into line management, Quality, Project Leadership or a variety of other positions, Parexel prides itself on career opportunities for our employees.

This role may be subject to government and/or customer requirements regarding vaccination against COVID-19 that are more stringent than Parexel policy. Accordingly, successful applicants may need to be either vaccinated against COVID-19 or have an approved religious or medical exemption. Employment is contingent on disclosure of your COVID-19 vaccination status and, if relevant, proof of vaccination.

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