What are the responsibilities and job description for the Sub-Investigator position at Austin Clinical Trial Partners?
Company 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