Clinical Research Coordinator II - Surgery

About the role

Scheduled Hours 40
Position Summary
Affords support to investigators in managing complex clinical research studies; may oversee multiple studies concurrently, serving as a liaison between the institution, sponsors, community, and study participants; oversees and maintains all phases of study protocols as mandated by sponsors to ensure compliance.

Primary Duties & Responsibilities

• Develops and discusses plans for research projects and interprets study results;
  Prepares manuscripts and grant proposals for publication and submission to sponsors;
  Prepares amendments to protocols and study designs as necessary.
• Coordinates the creation of forms, questionnaires, and research techniques;
  Writes instructional manuals for study progress, data collection, and coding;
  Reviews journals, abstracts, and scientific literature to stay updated on advancements and to inform future studies.
• Manages and ensures compliance with study protocols and regulatory agency guidelines;
  Establishes record-keeping systems;
  Makes assessments and determinations regarding participant progress;
  Analyzes and investigates adverse events;
  Notifies physicians of issues, stops participant inclusion, and adjusts protocols as needed.
• Serves as a liaison with funding or sponsoring agencies;
  Evaluates and interprets collected clinical data;
  Prepares presentations and reports detailing progress trends and recommendations.

Working Conditions

Job Location/Working Conditions
Patient care setting.
Physical Effort Typically sitting at desk or table.
Equipment Office equipment.

Education

Required Qualifications
Bachelor’s degree or equivalent combination of education and experience.

Skills

Not Applicable

Work Experience

Minimum 2 years of clinical research experience.

Other

Basic Life Support certification from the American Heart Association or American Red Cross is required.