Study Design Specialist (part-time)

CRIO; United States; On-site; USD 28,000 - 41,000; Part time

Job summary

CRIO is seeking a Study Design Specialist to build comprehensive eSource from protocols and eCRFs, and perform post-build QC reviews within the CRIO platform. This role requires attention to detail and the ability to mentor teammates while ensuring accurate data capture across complex trials.

The candidate will adapt templates to protocol requirements, manage multiple studies, and collaborate with cross-functional teams to deliver high-quality, on-time results.

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.

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.

Skills

eSource and QC design experience

Research coordination

Detail-oriented

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.
• Strong people skills.
• Detail-oriented with solid time management skills.
• Well-organized, capable of establishing priorities, and executing tasks efficiently.

Equal Employment Opportunity

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.

Join us at CRIO and be part of a dynamic team dedicated to revolutionizing the clinical research industry.

Benefits

This is a part time role:

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