Clinical Research Physician - Internal Medicine
Behavioral Health Market Context
Apply Nowvia Marit Health
Benefits
Dental CoverageHealth Insurance
Job Description
and ensure the quality of assigned studies, focusing on participant safety and ethical execution of trials.
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
Responsibilities
• Ensure the medical well-being and safety of study participants through safe performance and 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 into 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 involved in protocol training for staff
• Participate in Investigator Meetings (IMs) and continuing education activities to maintain current knowledge of recruitment affairs and issues
Benefits
• 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
Requirements
• MD or DO degree
• Active physician license (in good standing) in the state of practice for this role
• Experience with clinical trials
• Board certification in area of specialty
• CPR required / ACLS preferred
• Clinical skills and clinical procedures based in 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
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
Responsibilities
• Ensure the medical well-being and safety of study participants through safe performance and 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 into 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 involved in protocol training for staff
• Participate in Investigator Meetings (IMs) and continuing education activities to maintain current knowledge of recruitment affairs and issues
Benefits
• 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
Requirements
• MD or DO degree
• Active physician license (in good standing) in the state of practice for this role
• Experience with clinical trials
• Board certification in area of specialty
• CPR required / ACLS preferred
• Clinical skills and clinical procedures based in 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
Qualifications
- •MD or DO degree
- •Active physician license (in good standing) in the state of practice for this role
- •Experience with clinical trials
- •Board certification in area of specialty
- •Clinical skills and clinical procedures based in 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
Benefits
- •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
Responsibilities
- •This role, designated as a Principal Investigator, involves conducting and coordinating daily clinical trial activities in accordance with ICH/FDA/GCP guidelines, local regulations, and study protocols
- •The physician will provide clinical oversight and ensure the quality of assigned studies, focusing on participant safety and ethical execution of trials
- •Strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine
- •Ensure the medical well-being and safety of study participants through safe performance and 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 into 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 involved in protocol training for staff
- •Participate in Investigator Meetings (IMs) and continuing education activities to maintain current knowledge of recruitment affairs and issues
More Jobs
- Physical Therapist - PRNat Therapy Management Corporation
- Registered Behavior Technician (RBT) - Glenrock, Wyomingat Soliant
- Licensed Marriage and Family Therapist - Onsite or Remote (LMFT, LMFTS, or LCMFT)at Therapymatch Inc. (DBA Headway)
- Remote Paid Study Participant – Flexible Schedule (Earn Up to $750/Week)at Apex Focus Group Inc.
- Intern Behavior Therapistat Achieve Beyond
- BCBA — Clinical Leader, Mentorship & Pathat Action Behavior Centers
- In-Home RBT: Flexible Hours & Growth Opportunitiesat Skillful Steps ABA
- Licensed Mental Health Therapist - Onsite or Onlineat Therapymatch Inc. (DBA Headway)
- Speech Therapist SLP for Home Healthat FeldCare Connects
- Work with Kids! Registered Behavior Technician (RBT) / BCAT / ABAT – Part-Timeat Behavia Therapy