Clinician, Clinical Assessment Technologies - México - Worldwide Clinical Trials, LLC

Descripción

Who we are

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers. Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us

What Clinical Assessment Technologies does at Worldwide

Within the Clinical Assessment Technologies Department, the Clinician is responsible for all aspects of assigned projects that include clinical assessment, training development and data review for Worldwide Clinical Trials, Inc. (Worldwide). The Clinician works under the direction of the Director, Clinical Assessment Technologies (CAT).

What you will do

Tasks may include but are not limited to:

• The Clinician is responsible for reviewing study specific assessment-related data, as defined in the training plan, to determine eligibility of subjects and contact sites for clarification of data and results as well as being responsible for tracking the data reviews and monthly reporting to the sponsor and study team
• Assist in the review of eCOA/ePRO specifications and engages in User Acceptance Testing of equipment and programs. Communicates with study site staff regarding data quality issues.
• Conducts patient interviews, prepares scoring rationale, and coordinates establishment of score ranges. Reviews and provides feedback on protocol/CRF
• Attends regular client meetings, and attends Investigators' Meetings to assist with direct execution of training as appropriate. Travels to sites for motivational visits and monitoring of clinical assessments, as appropriate
• Collaborates internally and externally to ensure appropriate study design. Writes and QCs final reports, white papers and other scientific text

What you will bring to the role

• Demonstrable knowledge of operational aspects Phase I-IV clinical research and experience working with a Contract Research Organization/Rater Training Organization
• The ideal candidate should also have experience in a startup situation and building or implementing databases, project plans, as well as standardized processes and procedures
• Competency conducting patient interviews
• Knowledgeable about placebo response mitigation through various training techniques

Your experience

• Minimum of earned Master's Degree, M.D., Ph.D., PsyD, Pharm.D., in healthcare-related field, with one year of clinical experience, which includes administration of psychiatric and/or cognitive scales OR Bachelor's in healthcare-related field or RN with minimum 3 years of clinical experience, which includes administration of psychiatric and/or cognitive scales.Minimum 5 year's experience working at sites which may include CRO, rater training organizations, clinical trial sites, or biotech related industries.
• Willingness to travel and maintain flexible schedule
• Clear understanding of best business practices with respect to rater training, methodologies, and corporate discipline
• The Clinician must have experience with clinical research and the utilization of clinical assessment measures

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at For more information on Worldwide, visit or connect with us on LinkedIn.