Principle Investigator- Family Medicine Physician
85,318–200,000 a year
Behavioral Health Market Context
Apply Nowvia Glassdoor
Job Description
r clinical research, a strong background in family medicine, and a commitment to excellence in patient care and scientific discovery. This paid position offers an exciting opportunity to shape the future of family medicine through rigorous research, collaboration, and leadership.
Duties
• Lead and oversee all aspects of clinical research projects related to family medicine, ensuring adherence to FDA regulations, Good Clinical Practice (GCP), and HIPAA guidelines.
• Design, implement, and manage clinical trials involving patient monitoring, tissue culture, molecular biology assays, and other laboratory techniques such as Western blot, ELISA, PCR, flow cytometry, chromatography, and protein purification.
• Coordinate multidisciplinary teams including research staff, clinicians, laboratory technicians, and external partners to ensure smooth project execution.
• Review and validate documentation including study protocols, case report forms, data analysis plans using R, SAS, Python, or other statistical tools.
• Conduct patient assessments and monitor clinical trial participants for safety and efficacy outcomes.
• Ensure compliance with FDA regulations and ICH GCP standards throughout all phases of research.
• Oversee laboratory procedures involving cell culture, transfection techniques, tissue culture, microscopy, animal physiology studies, and assay development within a research laboratory environment.
• Maintain meticulous records of experimental procedures, results, and regulatory documentation; review documentation for accuracy and completeness.
• Foster collaborative relationships with academic institutions and industry partners to advance research initiatives in family medicine.
Experience
• Extensive experience leading clinical trials within a family medicine or primary care setting with a solid understanding of FDA regulations and GCP standards.
• Proven expertise in molecular biology techniques such as tissue culture, protein purification, Western blotting, PCR, ELISA, flow cytometry, chromatography, and cell transfection methods.
• Strong background in clinical research methodologies including patient monitoring and safety assessments.
• Demonstrated proficiency with statistical software such as SAS or R; experience with Python is a plus.
• Prior experience reviewing scientific documentation and ensuring regulatory compliance in clinical trials.
• Familiarity with HIPAA regulations related to patient data privacy and security.
• Hands-on laboratory experience in cell biology techniques including microscopy and mammalian cell culture.
• Knowledge of FDA regulations governing clinical research involving human subjects; certification in ICH GCP is highly desirable.
• Background in animal physiology studies or related biomedical research is an advantage. Join us as we push the boundaries of family medicine through innovative research that impacts communities worldwide! This role offers a unique blend of clinical leadership and scientific discovery—perfect for driven professionals eager to make a meaningful difference in healthcare innovation.
Pay: $85,318.30 - $200,000.00 per year
Work Location: In person
Duties
• Lead and oversee all aspects of clinical research projects related to family medicine, ensuring adherence to FDA regulations, Good Clinical Practice (GCP), and HIPAA guidelines.
• Design, implement, and manage clinical trials involving patient monitoring, tissue culture, molecular biology assays, and other laboratory techniques such as Western blot, ELISA, PCR, flow cytometry, chromatography, and protein purification.
• Coordinate multidisciplinary teams including research staff, clinicians, laboratory technicians, and external partners to ensure smooth project execution.
• Review and validate documentation including study protocols, case report forms, data analysis plans using R, SAS, Python, or other statistical tools.
• Conduct patient assessments and monitor clinical trial participants for safety and efficacy outcomes.
• Ensure compliance with FDA regulations and ICH GCP standards throughout all phases of research.
• Oversee laboratory procedures involving cell culture, transfection techniques, tissue culture, microscopy, animal physiology studies, and assay development within a research laboratory environment.
• Maintain meticulous records of experimental procedures, results, and regulatory documentation; review documentation for accuracy and completeness.
• Foster collaborative relationships with academic institutions and industry partners to advance research initiatives in family medicine.
Experience
• Extensive experience leading clinical trials within a family medicine or primary care setting with a solid understanding of FDA regulations and GCP standards.
• Proven expertise in molecular biology techniques such as tissue culture, protein purification, Western blotting, PCR, ELISA, flow cytometry, chromatography, and cell transfection methods.
• Strong background in clinical research methodologies including patient monitoring and safety assessments.
• Demonstrated proficiency with statistical software such as SAS or R; experience with Python is a plus.
• Prior experience reviewing scientific documentation and ensuring regulatory compliance in clinical trials.
• Familiarity with HIPAA regulations related to patient data privacy and security.
• Hands-on laboratory experience in cell biology techniques including microscopy and mammalian cell culture.
• Knowledge of FDA regulations governing clinical research involving human subjects; certification in ICH GCP is highly desirable.
• Background in animal physiology studies or related biomedical research is an advantage. Join us as we push the boundaries of family medicine through innovative research that impacts communities worldwide! This role offers a unique blend of clinical leadership and scientific discovery—perfect for driven professionals eager to make a meaningful difference in healthcare innovation.
Pay: $85,318.30 - $200,000.00 per year
Work Location: In person
Qualifications
- •Extensive experience leading clinical trials within a family medicine or primary care setting with a solid understanding of FDA regulations and GCP standards
- •Proven expertise in molecular biology techniques such as tissue culture, protein purification, Western blotting, PCR, ELISA, flow cytometry, chromatography, and cell transfection methods
- •Strong background in clinical research methodologies including patient monitoring and safety assessments
- •Prior experience reviewing scientific documentation and ensuring regulatory compliance in clinical trials
- •Familiarity with HIPAA regulations related to patient data privacy and security
- •Hands-on laboratory experience in cell biology techniques including microscopy and mammalian cell culture
- •Background in animal physiology studies or related biomedical research is an advantage
Benefits
- •Pay: $85,318.30 - $200,000.00 per year
Responsibilities
- •This pivotal role combines clinical expertise with research leadership, driving forward studies that improve patient outcomes and advance medical knowledge
- •The ideal candidate will possess a passion for clinical research, a strong background in family medicine, and a commitment to excellence in patient care and scientific discovery
- •This paid position offers an exciting opportunity to shape the future of family medicine through rigorous research, collaboration, and leadership
- •Lead and oversee all aspects of clinical research projects related to family medicine, ensuring adherence to FDA regulations, Good Clinical Practice (GCP), and HIPAA guidelines
- •Design, implement, and manage clinical trials involving patient monitoring, tissue culture, molecular biology assays, and other laboratory techniques such as Western blot, ELISA, PCR, flow cytometry, chromatography, and protein purification
- •Coordinate multidisciplinary teams including research staff, clinicians, laboratory technicians, and external partners to ensure smooth project execution
- •Review and validate documentation including study protocols, case report forms, data analysis plans using R, SAS, Python, or other statistical tools
- •Conduct patient assessments and monitor clinical trial participants for safety and efficacy outcomes
- •Ensure compliance with FDA regulations and ICH GCP standards throughout all phases of research
- •Oversee laboratory procedures involving cell culture, transfection techniques, tissue culture, microscopy, animal physiology studies, and assay development within a research laboratory environment
- •Maintain meticulous records of experimental procedures, results, and regulatory documentation; review documentation for accuracy and completeness
- •Foster collaborative relationships with academic institutions and industry partners to advance research initiatives in family medicine
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