UST-Clinical Hiring for Clinical Research Associate (1099 Contract) – Remote Based Job at Remote Full Time

UST-Clinical is a staffing organization who specializes in partnering with Pharma, Biotech, MedTech, and CRO organizations to fulfill their staffing needs. USTC is currently being retained to find multiple In-House (remote) Clinical Research Associates for a mid sized Sponsor.

What you’ll be doing:

CRA/Monitor responsible for monitoring remotely and on site.

You’ll also contribute by:

• Ensuring the validity, correctness, and completeness of clinical data reviewed and collected at assigned sites as dictated by trial protocol, ICH-GCP, and customer requirements.

You’ll be responsible for:

• Monitoring data — remotely, on site, and via other approved modes — with a focus on data integrity and patient safety, in accordance with specific country regulations.
• Overseeing the monitors at the CRO and reviewing trip reports.
• Preparing for and conducting qualification, study initiation, interim monitoring, and close-out visits at investigator sites.
• Gauging the quality of clinical deliverables and addressing quality issues with team members.
• Providing accurate and timely trip reports and records of hours worked.
• Managing query resolution with study sites and data management operations.
• Maintaining the project tracking system of subjects and site information.
• Participating in Investigators’ Meetings as assigned by Project Managers.
• Maintaining contact with investigator sites via telephone calls between visits.
• Ensuring adherence to study timelines and budgets.
• Identifying and escalating potential risks and identifying retraining opportunities for site study teams.
• Being a resource for other CRAs, mentoring CRA’s as appropriate and sharing knowledge and best practices.
• Participating in training offered to increase therapeutic knowledge and keeping current with regulations and FDA guidance.
• In specific countries or situations, assuming country-specific responsibilities and/or being named a subject-matter expert in one or more areas; e.g.: start-up, regulatory, site contracts, office management.
• Assuming additional duties on certain projects, such as clinical management for smaller or less complex studies.

You’ll need this to be considered:

• Bachelor’s Degree or equivalent experience required
• At least 2 years of CRA experience
• Ability to travel up to 20%

Seniority Level

Associate

Industry

• Pharma/Biotech
• Clinical Research

Employment Type

Full-time contract (1099)

Job Types: Full-time, Contract

Pay: $60.00 – $100.00 per hour

Schedule:

• Monday to Friday

Education:

• Bachelor’s (Preferred)

Experience:

• Clinical Trials: 5 years (Required)
• Clinical Research: 5 years (Required)

Work Location: Remote