Sub-Investigator

Austin Clinical Trial Partners; Austin (CO); On-site; USD 70,000 - 100,000; Full time

Job summary

Austin Clinical Trial Partners is looking for a full-time Sub-Investigator in Austin, Texas. The role involves conducting clinical trials while ensuring participant safety and compliance with regulatory standards. Ideal candidates will have expertise in patient care, familiarity with clinical trial protocols, and relevant qualifications. Strong organizational and communication skills are essential for success. Join a dedicated team to advance clinical research and patient care.

Qualifications

• Expertise in patient care, clinical assessment, and medical knowledge relevant to clinical trials.
• Familiarity with clinical trial protocols, regulatory guidelines, and Good Clinical Practice (GCP).
• Proficiency in documenting and maintaining accurate research records.
• Strong organizational, problem-solving, and communication skills.

Responsibilities

• Assist in conducting clinical trials by overseeing participant care.
• Ensure trials comply with regulatory standards.
• Support the Principal Investigator with protocol execution.
• Monitor patient safety and compliance during trials.

Skills

Patient care expertise

Clinical assessment knowledge

Organization skills

Problem-solving skills

Communication skills

Familiarity with clinical trial protocols

Proficiency in documentation

Education

PMHNP or PA-C with CAQ Psychiatry license

Job description

Austin Clinical Trial Partners is a dedicated research site focused on delivering high-quality medical care while advancing the field of clinical research. Supported by a team of experienced clinicians and research professionals, we collaborate with pharmaceutical sponsors to produce precise and timely data. Our mission is to serve patients effectively, ensuring their care and well-being remain our top priorities.

Role Description

This is a full-time, on-site Sub-Investigator role located in Austin, Texas. The Sub-Investigator will assist in conducting clinical trials by overseeing participant care, ensuring the trials comply with regulatory standards, and supporting the Principal Investigator with protocol execution. Responsibilities include assessing patient eligibility, monitoring safety and compliance, maintaining study documentation, and collaborating with research coordinators and other team members to ensure the successful execution of trials.

Qualifications

• Expertise in patient care, clinical assessment, and medical knowledge relevant to clinical trials
• Familiarity with clinical trial protocols, regulatory guidelines, and Good Clinical Practice (GCP)
• Proficiency in documenting and maintaining accurate research records and reporting adverse events
• Ability to collaborate with multidisciplinary teams, including Principal Investigators, sponsors, and coordinators
• Strong organizational, problem-solving, and communication skills
• PMHNP or PA-C with CAQ Psychiatry license, and prior experience in a clinical research setting.
• Familiarity with diagnostic and rating scales is a must
• Commitment to patient safety, ethical standards, and quality data collection
• Knowledge or experience in therapeutic areas being studied is a plus