Clinician, Clinical Assessment Technologies

hace 3 meses

Ciudad de México CDMX Worldwide Clinical Trials A tiempo completo

**Requisition Number**8336**

**Employment Type**:Regular**

**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 over 3,500+ 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.

**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**
- 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.

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