Clinical Trials Specialist (Neurosurgery)

UT Health San Antonio; San Antonio (TX); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading health institution in San Antonio is seeking a candidate for clinical trial operations oversight. This role involves administering and organizing training programs, maintaining research protocol inventories, and performing technical reviews. Successful applicants will have a knowledge of clinical trial design and will possess strong communication skills. Experience in clinical research is essential, and proficiency with Microsoft Office is required. The position offers a collaborative environment with the medical teams.

Qualifications

• Knowledge of scientific concepts related to clinical trial design and analysis.
• Experience with data collection and management methodologies.
• Demonstrated verbal and written communication skills.

Responsibilities

• Administers and conducts training for clinical trial operations.
• Maintains records of training activities and program effectiveness.
• Compiles reports for regulatory agencies and internal departments.

Skills

Clinical Research Certification

Communication skills

Data management

Microsoft Office proficiency

Job description

Job Description

Under limited supervision, responsible for assisting with the administration, organization and implementation of trial operations, systems management, and training/education. Provides specialized and technical reviews of clinical trial research protocols, funding agreements and billing processes.

This position will gain extensive research experience by interacting with Neurosurgery and Neurocritical Care research and works collaboratively with the medical teams.

Responsibilities

• Administers, organizes and conducts training/educational programs in connection with clinical trial operations, systems and management.
• Maintains records of training activities, progress, and program effectiveness.
• Ensures distribution and maintains inventory required for execution of research protocol(s).
• Assists in the determination of guidelines for new protocols.
• Works effectively in fast-paced environments, making quick, informed decisions with confidence.
• Compiles reports, documents and correspondence for regulatory agencies, participating clinical trial sites and internal departments to monitor and evaluate progress.
• Collects and prepares data for various clinical trial related reports.
• Develops, coordinates and conducts training in collaboration with clinical trial subject matter experts.
• Serves as liaison between clinical trial management systems end users and management systems support team.
• Performs all other duties as assigned.

Preferred Certification/Skills

Clinical Research Certification with ACRP or SoCRA

Qualifications

• Knowledge of scientific concepts related to the design and analysis of clinical trials.
• Knowledge of data collection and management methodologies of clinical trial.
• Ability to demonstrate excellent written and verbal communication.
• Proficiency with computers, including Microsoft Office.

Required Skills

Two years (2) related experience is required.