Adams Clinical
InSite Clinical Research - Principal Investigator
Adams Clinical, Desoto, Texas, United States, 75115
Job Overview:
InSite Clinical Research is seeking a dedicated Psychiatrist to join our team. As a Principal Investigator specializing in psychiatry, you will lead and oversee clinical research studies focused on CNS disorders. The ideal candidate will provide compassionate care and support to patients dealing with mental health disorders. This position offers the opportunity to work in a rewarding environment where you can make a positive impact on individuals' lives.
Responsibilities:
Conduct patient assessments to diagnose mental health conditions.
Evaluate and screen potential subjects based on study eligibility criteria; perform other psychiatric evaluations as required.
Perform physical examinations as a part of clinical study procedures.
Provide ongoing assessments of study subjects including any potential adverse events, or serious adverse events and ensure proper reporting of such events.
Provide medical management of Adverse Events and emergent events as appropriate.
Evaluate and assess laboratory reports and ECGs.
Follow protocol requirements including concomitant medication allowances and review inclusion/exclusion criteria.
Complete all training for study specific psychometric rating scales assigned to Principal Investigator in a timely manner. Administer and score psychometric rating scales at patient visits according to schedule of assessments.
Complete protocol specific training as required per sponsor’s vendors to obtain certification to conduct testing and rating scales for specific protocols.
Conduct and document training for all delegated individuals tasked with performing any study specific activities in the study.
Complete all documentation, paper and electronic, as required per protocol.
Provide oversight and ensure proper delegation of duties to appropriate staff.
Provide and maintain updated study related documentation as required by the clinical research trial to ensure data integrity.
Evaluate and report safety reports, protocol noncompliance, and any other protocol specific reports.
Follow requirements for FDA form 1572.
Collaborate with operational and management team to ensure site goals are met.
Attend Investigator Meetings as needed (some travel may apply).
Maintain all required licenses.
Skills:
Strong knowledge of clinical research methodologies, regulatory requirements, and GCP.
Excellent analytical, organizational, and communication skills.
Strong patient care skills with a focus on empathy and understanding.
Proficiency in conducting thorough patient assessment.
Experience in providing therapy and mental health counseling.
Ability to work with diverse patient populations, including Geriatrics.
Knowledge of medical records management and documentation.
Qualifications:
Education: Valid MD or DO with a specialization in Psychiatry or Neurology.
Board Certification in psychiatry or in process of obtaining one.
Active DEA license, or able to obtain one.
Active license to practice medicine in the state of Texas, or ability to obtain one immediately.
Experience (highly preferred): Minimum of 2 years of experience in clinical research, with a focus on psychiatric studies and CNS disorders.
Salary:
$300,000 per year
Job Type:
Full-time
Benefits:
401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance
Medical Specialty:
Neurology
Psychiatry
Schedule:
In-person (DeSoto, TX 75115), 8-to-10-hour day shift Monday through Friday with weekends as needed.
Work Location:
In person
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InSite Clinical Research is seeking a dedicated Psychiatrist to join our team. As a Principal Investigator specializing in psychiatry, you will lead and oversee clinical research studies focused on CNS disorders. The ideal candidate will provide compassionate care and support to patients dealing with mental health disorders. This position offers the opportunity to work in a rewarding environment where you can make a positive impact on individuals' lives.
Responsibilities:
Conduct patient assessments to diagnose mental health conditions.
Evaluate and screen potential subjects based on study eligibility criteria; perform other psychiatric evaluations as required.
Perform physical examinations as a part of clinical study procedures.
Provide ongoing assessments of study subjects including any potential adverse events, or serious adverse events and ensure proper reporting of such events.
Provide medical management of Adverse Events and emergent events as appropriate.
Evaluate and assess laboratory reports and ECGs.
Follow protocol requirements including concomitant medication allowances and review inclusion/exclusion criteria.
Complete all training for study specific psychometric rating scales assigned to Principal Investigator in a timely manner. Administer and score psychometric rating scales at patient visits according to schedule of assessments.
Complete protocol specific training as required per sponsor’s vendors to obtain certification to conduct testing and rating scales for specific protocols.
Conduct and document training for all delegated individuals tasked with performing any study specific activities in the study.
Complete all documentation, paper and electronic, as required per protocol.
Provide oversight and ensure proper delegation of duties to appropriate staff.
Provide and maintain updated study related documentation as required by the clinical research trial to ensure data integrity.
Evaluate and report safety reports, protocol noncompliance, and any other protocol specific reports.
Follow requirements for FDA form 1572.
Collaborate with operational and management team to ensure site goals are met.
Attend Investigator Meetings as needed (some travel may apply).
Maintain all required licenses.
Skills:
Strong knowledge of clinical research methodologies, regulatory requirements, and GCP.
Excellent analytical, organizational, and communication skills.
Strong patient care skills with a focus on empathy and understanding.
Proficiency in conducting thorough patient assessment.
Experience in providing therapy and mental health counseling.
Ability to work with diverse patient populations, including Geriatrics.
Knowledge of medical records management and documentation.
Qualifications:
Education: Valid MD or DO with a specialization in Psychiatry or Neurology.
Board Certification in psychiatry or in process of obtaining one.
Active DEA license, or able to obtain one.
Active license to practice medicine in the state of Texas, or ability to obtain one immediately.
Experience (highly preferred): Minimum of 2 years of experience in clinical research, with a focus on psychiatric studies and CNS disorders.
Salary:
$300,000 per year
Job Type:
Full-time
Benefits:
401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance
Medical Specialty:
Neurology
Psychiatry
Schedule:
In-person (DeSoto, TX 75115), 8-to-10-hour day shift Monday through Friday with weekends as needed.
Work Location:
In person
#J-18808-Ljbffr