Clinical Research Assistant: Study Coordination & Data

Union-Community-Care; Pennsylvania; On-site; USD 44,000 - 52,000; Full time

Job summary

Union Community Care is seeking a Research Assistant to perform day-to-day study activities across performance sites. You will obtain informed consent, conduct assessments, enter data, and manage participant follow-up and compensation.

You will support regulatory and quality monitoring and participate in team conference calls as needed. Responsibilities include explaining the study, coordinating visits, tracking participants, maintaining data integrity, and ensuring protocol and federal

Qualifications

• Bachelor’s degree in human services related field or equivalent.
• One year of experience in health care or human services related fields.
• Strong interpersonal skills and ability to work independently and as a team member.
• Meticulous attention to detail; organized, efficient, and able to handle competing priorities.
• Previous project-related work including prior work with study population within medical/clinical settings, conducting standardized assessments.
• Prior research experience and some understanding of research procedures.

Responsibilities

• Explain study to participants, obtain informed consent and schedule visits.
• Conduct research interviews at primary care study sites and manage study visits.
• Track participant flow and update tracking logs accurately.
• Review data entries for accuracy and resolve data queries.
• Maintain study files and ensure participant confidentiality and regulatory compliance.
• Assist with regulatory documents and overall project operations.

Skills

Interpersonal skills

Attention to detail

Time management

Teamwork

Education

Bachelor's degree in human services related field

Job description

Union Community Care is seeking a Research Assistant to perform day-to-day study activities across performance sites. You will obtain informed consent, conduct assessments, enter data, and manage participant follow-up and compensation.

You will support regulatory and quality monitoring and participate in team conference calls as needed. Responsibilities include explaining the study, coordinating visits, tracking participants, maintaining data integrity, and ensuring protocol and federal