Clinical Research Physician - Metabolic or Hepatology - part time (16 hours per week) at Alcanza Clinical Research Sugar Land, TX

Benefits

Qualifications

• •Skills, Knowledge And Expertise Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role
• •Clinical research experience is required
• •Board certification in area of specialty required
• •Required Skills Clinical skills and clinical procedures based on area of specialty
• •Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm)
• •Must possess strong organizational skills, attention to detail, and math proficiency
• •Well-developed written and verbal communication skills
• •Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers
• •Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities
• •Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic
• •Must possess a high degree of urgency, self-motivation, integrity and dependability
• •Ability to work independently to identify problems and implement solutions
• •Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines
• •10 more items(s)

Responsibilities

• •The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes
• •Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site
• •Key Responsibilities Essential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance Evaluates and assesses participants to ensure only eligible participants enroll into the trials
• •Participates and engages in successful delivery and retention of study participants
• •Interacts positively and collaboratively with sponsors, clients and team members
• •Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs
• •Actively involved in protocol training for staff
• •Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues
• •Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company
• •6 more items(s)