Clinical Research IO (CRIO) is a fast-moving Boston-based company working to transform the clinical research industry with the latest in cloud and tablet technology. At CRIO, our talented people are making an impact throughout clinical trials. We are looking to build out our Study Design team with solid, well-grounded individuals who are experienced in quality control. Reporting to the Study Design Manager, the Study Design Reviewer at CRIO will provide an extensive review of the eSource study build to ensure it will capture all required data necessary for accurate and complete collection of data. CRIO handles a wide variety of conditions including cardiovascular, dermatological, endocrine, gastrointestinal, mental health, musculoskeletal, oncological, reproductive, respiratory, urinary, SARS-COV-2 vaccinations/therapeutics, and surgical devices. The reviewer will be providing the study designer with detailed feedback of the build as well as communicating with the client on final revisions of the build.

ESSENTIAL JOB FUNCTIONS:

● Performs quality check on study templates to ensure consistency to the protocol as well as internal standards

● Provides feedback for study designers to ensure clinically accurate templates for clinical trial procedures

● Revises study builds according to clients’ comments

● Ensures final study build reflects best evidence-based practices

● Integrates Clinical Trial Agreements into the financial module for specific builds

● Fields study design questions from clients through a conferencing platform

Requirements

● Strong ability to interpret clinical trial protocols, clinical trial agreements and source documents
● Knowledge of eSource design tools

● Strong knowledge of medical terminology and procedures

● Committed to providing excellent customer service

● Communicates and collaborates well with other team members

● Exhibits excellent written and oral communication

● Solid time management skills to meet deadlines in a fast-paced environment and monthly benchmarks

● Proven ability to deliver on delegated work efficiently

● Strong attention to detail

Well organized, ability to multitask and prioritize tasks

QUALIFICATIONS:

Education

● BS in medical or sciences field (preferred or equivalent experience)

Experience/Training:

● Healthcare experience of at least 1 year

● Research coordinator experience of at least 1 year

● Previous experience with Quality Control

PREFERRED QUALIFICATIONS:

● Clinical Research Coordinator (CRC)

Benefits

• Work from anywhere
• Unlimited PTO
• 401k company match
• Healthcare
• Dental
• Vision
• Life insurance
• Professional development

At CRIO, equality is a core tenet of our culture. We are committed to building an inclusive global team that represents a variety of backgrounds, perspectives, beliefs, and experiences. The more diverse we are, the richer our community and the broader our impact. Employment decisions are made on the basis of job-related criteria without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other classification protected by applicable law.