Physician

Synectics Inc.; Riverside (CA); On-site; USD 140,000 - 210,000; Full time

Job summary

Synectics Inc. is seeking a Clinical Research Physician Investigator (PI) to lead study conduct, oversee Sub-Investigators, and ensure compliance with FDA/IRB protocols.

The role involves direct participant assessment, data integrity, and coordinating with monitoring visits in a dynamic clinical research environment. The candidate should have 1–2 years of PI/clinical research experience, active medical license, and preferred experience in internal medicine or related specialties.

Qualifications

• 1-2 years of Principal Investigator/clinical research experience preferred.
• 1-2 years of clinical practice in Internal Medicine, Behavioral Neurology, Family Medicine, Endocrinology, Gastroenterology, or Liver/Hepatology preferred.
• Current and active physician license required.
• Board Certification preferred.

Responsibilities

• Develop and maintain expert knowledge of study-related activities and protocols.
• Assume investigator responsibilities and obligations per Title 21 CFR Part 312 and FDA Form 1572.
• Adhere to study protocols, FDA regulations and GCP requirements.
• Maintain confidentiality of study sponsors and clinical trial information.
• Perform study-related procedures including physical exams, informed consent, history review, adverse event assessment, and vital signs collection.
• Review laboratory, imaging, and biopsy findings; assist with monitoring visits.
• Screen and recruit participants; coordinate care and visits.

Skills

Strong communication

Bilingual English/Spanish

Organizational skills

Attention to detail

Interpersonal skills

Adaptability

Mathematical/analytical skills

Computer skills

MS Office/Enterprise software

Tools

Microsoft Office

Web browsers

Web-based enterprise software

Job description

About The Job

Join a dynamic team focused on advancing medical discovery through high-quality clinical research. The organization conducts rigorous clinical research studies designed to improve patient care and contribute to advancements in healthcare.

About The Job

Join a dynamic team focused on advancing medical discovery through high-quality clinical research. The organization conducts rigorous clinical research studies designed to improve patient care and contribute to advancements in healthcare.

Summary

The Clinical Research Clinical Research Physician Investigator / Principal Investigator (PI)

The PI Assumes Overall Responsibility For Study Conduct, Including

• Personally conducting or supervising research activities.
• Ensuring delegated tasks are performed by appropriately qualified individuals based on education, training, and experience.
• Protecting the rights, safety, and welfare of study participants.
• Ensuring research is conducted in compliance with federal regulations, state laws, organizational policies, and SOPs.
• Ensuring studies follow the IRB-approved protocol.
• Maintaining the accuracy, security, and integrity of research data and analysis.

Duties And Responsibilities

• Develop and maintain expert knowledge of study-related activities and protocols.
• Assume investigator responsibilities and obligations in accordance with Title 21 CFR Part 312 and FDA Form 1572.
• Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) requirements.
• Maintain confidentiality of study sponsors and clinical trial information.
• Perform study-related procedures, including physical examinations, informed consent, medical history review, adverse event assessment, test article handling, appointment scheduling, medical records review, treatment coordination, vital sign collection, and participant health assessments.
• Review and adjudicate laboratory, imaging, and biopsy findings.
• Assist with preparation for study monitoring visits.
• Conduct participant screening and recruitment.
• Provide occasional weekend coverage to facilitate study visits according to protocol requirements.
• Provide after-hours telephone coverage as needed.
• Oversee Sub-Investigators and clinical research/recruitment staff.

Education & Experience

1-2 years of Principal Investigator/clinical research experience preferred.

1-2 years of clinical practice in one or more of the following areas preferred:

• Internal Medicine
• Behavioral Neurology
• Family Medicine
• Endocrinology
• Gastroenterology
• Liver Disease/Hepatology

Licensure & Certification

• Current and active physician license required.
• Board Certification preferred.

Knowledge, Skills & Abilities

• Strong written and verbal communication skills.
• Bilingual English/Spanish strongly preferred.
• Excellent organizational and attention-to-detail skills.
• Strong interpersonal and communication skills.
• Professional, positive, and patient-focused demeanor.
• Ability to adapt to changing priorities.
• Strong mathematical and analytical skills.
• Excellent computer skills.
• Proficiency with Microsoft Office, web browsers, and web-based enterprise software.

Work Environment & Physical Requirements

• Work may be performed in an office, laboratory, and/or clinical environment.
• May involve exposure to biological fluids and bloodborne pathogens.
• Personal protective equipment may be required, including protective eyewear, garments, and gloves.
• Occasional domestic or international travel may be required.
• Ability to remain upright or stationary for 6-10 hours per day.
• Frequent mobility is required.
• Occasional squatting, kneeling, or bending.
• Ability to lift and carry medical equipment or other objects weighing approximately 20-50 lbs.