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Clinician, Clinical Assessment Technologies - Europe - Home-based

Employer
Worldwide Clinical Trials
Location
Nottingham, United Kingdom;Homeworking
Salary
Competitive
Start date
10 Jan 2023
Closing date
8 Feb 2023

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Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

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.

We are Worldwide Clinical Trials, and we are a global team of almost 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

What you will do
  • Development and management of training plans, data review plans, schedules, and timelines.
  • Development and oversight of data review and dissemination of data review.
  • Review study-specific assessment-related data, as defined in the training plan, to determine the eligibility of subjects and contact sites for clarification of data as well as results of the reviews.
  • Track the data reviews and monthly report to the sponsor and study team; review rater data to determine if rater or data errors have occurred, track, report and reconcile the data errors.
  • Conduct patient interviews, prepares scoring rationale, and coordinate the establishment of score ranges.
  • Research into scale acquisition and coordination with Worldwide and the sponsor to acquire licenses.
  • Assist in the review of eCOA/ePRO specifications and engages in User Acceptance Testing of equipment and programs.
  • Review and provide feedback on protocol/CRF.
  • Attends regular client meetings, and attends Investigators’ Meetings to assist with the direct execution of training as appropriate.
  • Travels to sites for motivational visits and monitoring of clinical assessments, as appropriate
  • Writes and QCs final reports, white papers, and other scientific texts.
  • Conducts training for Worldwide staff and investigators as appropriate and participates in training and/or ongoing synchronization of external Clinical Experts.


What you will bring to the role
  • Strong organizational and management skills are essential attributes.
  • Excellent written and verbal communication skills to clearly and concisely present information.
  • Strong interpersonal skills in a fast-paced, deadline-oriented, and changing environment.
  • Excellent ability to handle multiple tasks and many administrative details in a fast-paced and constantly changing environment.
  • Ability to exercise sound judgment and make decisions independently.
  • Competency conducting patient interviews.
  • Knowledge of Clinician and Patient Reported Outcomes in multiple indications.
  • Knowledgeable about placebo response mitigation through various training techniques.
  • Ability to research new measures, across indications, and develop appropriate training materials for such measures.
  • Comfortable using innovative technologies to enhance training programs; including but not limited to: training video development, eCOA/ePRO technologies, and actigraphy
  • Willingness to travel.
  • Proficiency in all MS-Office applications including Microsoft Word, Excel, and PowerPoint.


Your background
  • Minimum 5 years’ experience working at sites which may include CRO, rater training organizations, clinical trial sites, or biotech-related industries.
  • Minimum of earned Master’s Degree, M.D., Ph.D., PsyD, Pharm.D., in a healthcare-related field, with one year of clinical experience, which includes administration of psychiatric and/or cognitive scales OR Bachelor’s in the healthcare-related field or RN with minimum 3 years of clinical experience, which includes administration of psychiatric and/or cognitive scales.
  • Demonstrable knowledge of operational aspects of Phase I-IV clinical research and experience working with a Contract Research Organization/Rater Training Organization.


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.

Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers!

#LI-MP1 #LI-Remote

Company

Find out more about working for our company

Worldwide Clinical Trials -hub-button

Brief Company Description; 

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.

We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

 

Company info
Website
Mini-site
Worldwide Clinical Trials
Telephone
+44 115 956 7711
Location
1st Floor Waterfront House
Beeston Business Park
Beeston
Nottingham
Nottinghamshire
NG9 1LA
United Kingdom

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