Clinical Research Physician - Psychiatrist - Part Time - Monday and Wednesdays needed

Alcanza Clinical Research•Katy, TX

11d•Onsite

About The Position

Alcanza is a growing, multi-site, multi-phase clinical research company conducting Phase I-IV studies across therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. The Clinical Research Physician serves as a Principal Investigator, conducting and coordinating daily clinical trial activities in accordance with ICH/FDA/GCP guidelines, local regulations, study protocols, and company policies and processes. Working with local and central teams, the physician provides clinical oversight and supports the quality of assigned studies at the site. This is a part-time role based at Olympus in Katy, Texas, with work needed on Mondays and Wednesdays.

Requirements

MD or DO degree.
Active physician license in good standing in the state of practice for this role.
At least 2 years of experience in a medical research environment, or an equivalent combination of education and experience.
Board certification in the area of specialty.
CPR certification required.
Clinical skills and clinical procedures in the area of specialty.
Proficiency with MS Office, electronic health records, and web applications, and ability to type at least 40 words per minute.
Strong organizational skills, attention to detail, and math proficiency.
Well-developed written and verbal communication skills.
Well-developed interpersonal and listening skills, with the ability to work independently and collaboratively with coworkers, employees, subjects, managers, and external customers.
Ability to handle multiple tasks and adapt to changing workloads and priorities.
Professionalism, respect for others, self-motivation, and a strong work ethic.
High degree of urgency, self-motivation, integrity, and dependability.
Ability to identify problems and implement solutions independently.
Ability to handle sensitive information confidentially and professionally, in compliance with HIPAA guidelines.

Nice To Haves

ACLS certification preferred.
Bilingual English/Spanish proficiency highly preferred.

Responsibilities

Ensure the medical well-being and safety of study participants through safe performance and ethical execution of clinical trials, following FDA, ICH, NIH, GCP, and HIPAA guidelines, study protocols, and company policies and processes.
Provide overall site leadership focused on improving efficiencies, participant safety, and protocol, GCP, and regulatory compliance.
Evaluate and assess participants to ensure that only eligible participants enroll in trials.
Support successful delivery and retention of study participants.
Interact positively and collaboratively with sponsors, clients, and team members.
Record data and participant information accurately and in accordance with protocol guidelines and GCPs.
Participate actively in protocol training for staff.
Attend Investigator Meetings and continuing education activities to maintain current knowledge of recruitment affairs and issues.
Perform other duties as assigned, requested, or required based on participant, protocol, or company needs.