Study Design Specialist (part-time)

CRIO, Inc.; United States; Remote; USD 60,000 - 80,000; Part time

Job summary

A health tech company, CRIO, is looking for a part-time Study Design Specialist to create comprehensive builds in their platform. This role involves developing eSource from protocols and conducting quality control reviews while mentoring team members. Applicants should possess a BS in a medical or sciences field, along with relevant healthcare experience.

Qualifications

• At least 1 year of healthcare experience.
• Experience with eSource and QC design in CRIO or other systems.
• Ability to interpret clinical trial protocols, and source documents.

Responsibilities

• Create comprehensive study builds using protocols and eCRF guidelines.
• Manage complex trials and ensure appropriate data capture.
• Mentor and train current and new employees.

Skills

Detail-oriented

Time management

Organizational skills

Education

BS in medical or sciences field

Job description

CRIO (Clinical Research IO) is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system and a single source of clinical data capture. Our modules allow sites to capture data electronically in real-time, providing data managers and monitors with enhanced transparency, and enabling remote monitoring by sponsors and CROs.

CRIO’s eSource and CTMS system is a leading, modern, enterprise platform built for clinical research sites. Since CRIO’s launch in 2016, CRIO has established the leading brand position in eSource and has won close to 50% of the emerging class of enterprise-grade site networks, many of whom are backed by institutional investors such as VC, PE and corporations. CRIO has achieved the attached metrics, all with little to no serious outbound sales or marketing.

The Study Design Specialist is responsible for creating comprehensive study builds from start to finish in the CRIO platform. This includes developing eSource from protocols and eCRFs, and conducting post-build quality control reviews This individual will be considered an industry expert on the CRIO eSource module.

Responsibilities:

• Utilize protocols, eCRF guidelines, pharmacy manuals, lab manuals, and other source documents to produce comprehensive builds for clients.
• Complete client-requested edits and customizations.
• Manage complex trials to ensure all data is captured appropriately.
• Modify standard templates to comply with protocol requirements.
• Complete assignments on time.
• Mentor and train current and new CRIO employees.

Preferred Qualifications:

• Experience with eSource and QC design in CRIO or other eSource/CTMS systems.
• BS in medical or sciences field.
• Experience as a Research Coordinator, Site Director, or Source Designer is a plus.

Other Qualifications:

• At least 1 year of healthcare experience.
• Ability to interpret clinical trial protocols, and source documents.
• Knowledge of medical terminology and procedures.
• Detail-oriented with solid time management skills.
• Well-organized, capable of establishing priorities, and executing tasks efficiently.

Join us at CRIO and be part of a dynamic team dedicated to revolutionizing the clinical research industry. Apply today to embark on a rewarding career journey!

We’re proud to be an equal opportunity employer and welcome our employee’s differences, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or Veteran status. Difference makes us better. Join us.

This is a part time role:

Compensation Package - $20 an hour for all training and up to $450 for Study Design Build