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Sr. Clinical Trial Manager [US or Canada Remote] 83184

PRA Health Sciences

This is a Full-time position in Washington, DC posted October 25, 2021.

ICON plc is a world-leading healthcare intelligence and clinical research organisation.

From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

 

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

 

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success.

ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Qualifications

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 1-2 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 30%, required
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 1-2 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, and should not require, now or in the future, sponsorship for employment visa status.
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.

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)

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