Clinical Research Physician - Internal Medicine
Behavioral Health Market Context
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Benefits
Health InsuranceDental Coverage
Job Description
guidelines, study protocols, and company policies.
Practice Info
• Multi-site, multi-phase clinical research company
• Network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico
• Strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine
• Local and central team collaboration
Responsibilities
• Ensure medical well-being and safety of study participants through ethical execution of clinical trials, adhering to FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, and company policies
• Provide overall site leadership with a focus on enhancing efficiencies, patient safety, and protocol/GCP/regulatory compliance
• Evaluate and assess participants to ensure only eligible individuals enroll in trials
• Participate and engage in successful delivery and retention of study participants
• Interact positively and collaboratively with sponsors, clients, and team members
• Practice attention to detail in recording data and participant information, following protocol guidelines and GCPs
• Actively involve in protocol training for staff
• Participate in Investigator Meetings (IMs) and continuing education activities to maintain current knowledge of recruitment affairs and issues
Benefits
• Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire
• Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered
Shift & Schedule
• Part time - 16-24 hrs/week
Requirements
• MD or DO degree
• Active physician license (in good standing) in the state of practice for this role
• Board certification in area of specialty required
• CPR required
• 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)
• 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
Practice Info
• Multi-site, multi-phase clinical research company
• Network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico
• Strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine
• Local and central team collaboration
Responsibilities
• Ensure medical well-being and safety of study participants through ethical execution of clinical trials, adhering to FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, and company policies
• Provide overall site leadership with a focus on enhancing efficiencies, patient safety, and protocol/GCP/regulatory compliance
• Evaluate and assess participants to ensure only eligible individuals enroll in trials
• Participate and engage in successful delivery and retention of study participants
• Interact positively and collaboratively with sponsors, clients, and team members
• Practice attention to detail in recording data and participant information, following protocol guidelines and GCPs
• Actively involve in protocol training for staff
• Participate in Investigator Meetings (IMs) and continuing education activities to maintain current knowledge of recruitment affairs and issues
Benefits
• Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire
• Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered
Shift & Schedule
• Part time - 16-24 hrs/week
Requirements
• MD or DO degree
• Active physician license (in good standing) in the state of practice for this role
• Board certification in area of specialty required
• CPR required
• 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)
• 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
Qualifications
- •MD or DO degree
- •Active physician license (in good standing) in the state of practice for this role
- •Board certification in area of specialty required
- •CPR required
- •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)
- •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
Benefits
- •Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire
- •Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered
- •Shift & Schedule
- •Part time - 16-24 hrs/week
Responsibilities
- •This role involves conducting and coordinating daily clinical trial activities as a Principal Investigator, ensuring medical well-being and safety of study participants
- •The physician will drive clinical oversight and quality for assigned studies, adhering to ICH/FDA/GCP guidelines, study protocols, and company policies
- •Strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine
- •Local and central team collaboration
- •Ensure medical well-being and safety of study participants through ethical execution of clinical trials, adhering to FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, and company policies
- •Provide overall site leadership with a focus on enhancing efficiencies, patient safety, and protocol/GCP/regulatory compliance
- •Evaluate and assess participants to ensure only eligible individuals enroll in trials
- •Participate and engage in successful delivery and retention of study participants
- •Interact positively and collaboratively with sponsors, clients, and team members
- •Practice attention to detail in recording data and participant information, following protocol guidelines and GCPs
- •Actively involve in protocol training for staff
- •Participate in Investigator Meetings (IMs) and continuing education activities to maintain current knowledge of recruitment affairs and issues