Principal Investigator: Clinical Research Leader | CME & Benefits

Pinnacle Clinical Research- A Summit Solution; Riverview (CA); On-site; USD 150,000 - 230,000; Full time

Benefits offered by this job

401k

Medical insurance

Dental insurance

Vision insurance

Disability insurance

Life insurance

3 weeks PTO

13 paid holidays

CME allowance

Tranquility Room

Pinnacle Gym

Scrub voucher

Job summary

Pinnacle Clinical Research- A Summit Solution is seeking a Clinical Research Physician Investigator to oversee study conduct, ensure regulatory compliance, and supervise protocol-adherent activities. The role includes performing clinical procedures, informed consent, and data integrity checks in sponsor-driven trials.

Ideal candidates hold an MD with PI experience and are able to lead a team, manage recruitment, and ensure alignment with GCP and IRB plans in a fast-paced clinical setting.

Qualifications

• Current physician license and practicing credentials.
• Preference for board-certified physicians.
• Experience as a principal investigator preferred.

Responsibilities

• Review and maintain expert knowledge of study-related activities and protocols.
• Adhere to FDA regulations, GCP, and study protocols at all times.
• Maintain sponsor and clinical trial confidentiality.
• Perform procedures including examinations, informed consent, and data collection.
• Coordinate subject screening, recruitment, and visits per protocol.
• Provide after-hours coverage and occasional weekend support.
• Oversee Sub-Investigators and recruitment team.

Skills

Communication skills

Bilingual (English & Spanish)

Organizational skills

Attention to detail

People skills

Diplomatic communication

Interpersonal skills

Mathematical knowledge

Computer proficiency

Education

MD (Medical Doctor)

Board Certification preferred

Tools

Microsoft Office

Internet Explorer

Google Chrome

Mozilla Firefox

Web-based enterprise software

Job description

Pinnacle Clinical Research- A Summit Solution is seeking a Clinical Research Physician Investigator to oversee study conduct, ensure regulatory compliance, and supervise protocol-adherent activities. The role includes performing clinical procedures, informed consent, and data integrity checks in sponsor-driven trials.

Ideal candidates hold an MD with PI experience and are able to lead a team, manage recruitment, and ensure alignment with GCP and IRB plans in a fast-paced clinical setting.