Global Clinical Trial Manager

PRA Health Sciences; Myrtle Point (OR); Remote; USD 90,000 - 120,000; Full time

Job summary

A global healthcare company is seeking a Global Clinical Trial Manager to lead and coordinate clinical trials worldwide. The ideal candidate will have a background in life sciences with at least 4 years of clinical trial experience and strong communication skills. Responsibilities include managing trial execution, ensuring study compliance, and effective risk management to improve the lives of patients.

Benefits

Comprehensive benefits package

Continuous learning culture

Recognition programs

Qualifications

• Minimum of 4 years of clinical trial experience and 2 years of global clinical trial management experience.
• Broad experience working in life sciences or medically related field.
• Excellent communication and interpersonal skills to effectively work with cross-functional teams.

Responsibilities

• Lead, manage and coordinate clinical trials from study design to close out.
• Collaborate with Clinical Program Management teams for global execution of studies.
• Ensure effective study risk management across all areas of studies.

Skills

Clinical trial management

Communication skills

Risk management

Knowledge of ICH/GCP

Education

BA/BS/BSc or RN

Job description

Overview

As a Global Clinical Trial Manager, you will play a key role in improving the lives of patients by accelerating the development of our customers ' drugs and devices through innovative solutions. You will be a dedicated resource to one of our clients, embedded in their working environment, systems, and processes.

Responsibilities

What you will be doing:

• Primary point of contact to lead, manage and coordinate the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCP, international regulations and sponsor SOPs
• Collaborate with Clinical Program Management teams for global execution of studies
• Ensure effective study risk management in place across all areas of studies
• Oversee and maintain the quality and scientific integrity of clinical operations for studies at a global level
• Collaborate with cross-functional internal and external stakeholders to ensure timely and on budget execution of clinical trial deliverables
• Proactively identify and communicate appropriately the status of ongoing studies, identified risks, mitigation strategies, associated action plans and issue resolution measures to ensure timely and on budget execution of study deliverables

Qualifications

You are:

• Education: BA/BS/BSc or RN
• Minimum of 4 years of clinical trial experience and 2 years of global clinical trial management experience.
• Broad experience working in life sciences or medically related field, including general biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company).
• Excellent communication and interpersonal skills to effectively work with cross-functional teams.
• Knowledge of ICH/GCP and regulatory guidelines/directives.

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Benefits

Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.