**Requisition Number**8012**
**Employment Type**:Regular**
**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:_
- 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
- 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.
