Clinical Trial Manager (Home Based – US or Canada)

Job title: Clinical Trial Manager (Home Based – US or Canada)

Company: PRA Health Sciences

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Clinical Trial Manager (Home Based – US or Canada)

Job Locations (All) | US-Remote | Canada-Remote

Posted Date 8 hours ago(5/12/2021 2:43 PM)

ID 2021-76054

Overview

Do you want to watch clinical development change, or do you want to be the one to shape it?

Because we’re hoping you’re here for the latter.

Who are we?

We Are PRA Health Sciences. We provide innovative drug development solutions across all phases and therapeutic areas. But innovation just for the sake of innovation isn’t why we do it. Side by side with our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every day. It’s who we are. Innovating to help people is at the heart of our process, but it’s even more than that. It’s our privilege.

We are 20,000+ employees strong, operating in more than 90 countries. We are committed to saving lives, and we are constantly striving to be the best at what we do.

Who Are You?

You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.

Still here? Good. Because if this is you, we’d really like to meet you.

Responsibilities

What will you be doing?

As a Clinical Team Manager (CTM), you have a wide range of responsibilities. We’re including a few of the big ones. Primarily, you will work to achieve the most successful clinical trial possible. You will lead cross-functional teams with Project Management, Clinical Operations, and Regulatory Affairs, while understanding and managing client expectations. You will proactively identify, resolve/mitigate, and escalate risks or issues when necessary.

• Provide Project Oversight and Leadership for Clinical Deliverables
• Project Resourcing
• Quality – Training & Development
• Project Finance
• Customer Relations (Internal & External)

Qualifications

What do you need to have?

Level 2:

• Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (ie, registered nurse); or equivalent work experience, required
• 5+ years of clinical research experience, required
• 2+ years of experience in clinical trial management, strongly preferred
• 2+ years monitoring experience, strongly preferred
• Experience in managing complex or global trials, preferred
• Minimum 1 year oncology experience, preferred
• Minimum 1-2 years of experience leading Oncology cellular therapy trials, strongly preferred.
• Experience should include oversight of clinical trials using genetically-modified or somatic cell adoptive transfer in either autologous and/or allogeneic settings where cellular product logistics management was used.
• Experience in managing all trial components (start-up to database lock), preferred
• Experience in coaching/mentoring other CTMs, leading a team of CTMs, participating in departmental initiatives, preferred
• English fluency (ability to read, write, speak), required
• Travel of up to a maximum of 20-30% at times.
• To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

Level 3:

• Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (ie, registered nurse); or equivalent work experience, required
• 7+ years of clinical research experience, required
• 4-5+ years of experience in clinical trial management, strongly preferred
• 2+ years monitoring experience, strongly preferred
• Experience in managing complex or global trials, preferred
• Minimum 1 year oncology experience, preferred
• Minimum 1-2 years of experience leading Oncology cellular therapy trials, strongly preferred.
• Experience should include oversight of clinical trials using genetically-modified or somatic cell adoptive transfer in either autologous and/or allogeneic settings where cellular product logistics management was used.
• Experience in managing all trial components (start-up to database lock), preferred
• Experience in coaching/mentoring other CTMs, leading a team of CTMs, participating in departmental initiatives, preferred
• Experience in managing complex trials or global trials, preferred
• English fluency (ability to read, write, speak), required
• Travel of up to a maximum of 30%, required
• To qualify, applicants must be legally authorized to work in the United States or Canada, and should not require, now or in the future, sponsorship for employment visa status.

LOCATION: This position may be home-based or office-based, depending on location.

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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Expected salary:

Location: Canada

Job date: Fri, 14 May 2021 05:31:25 GMT