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Weekend Ethics Investigator Jobs (NOW HIRING)

Digital Remedy

Investigative Reporter

Reno, NV

Knowledge of broadcast journalism principles and ethics. * Proficiency with digital and social ... Work evenings, weekends, holidays, and extended hours as newsroom operations and breaking news ...

Hearst

Investigative Reporter/Producer

Pittsburgh, PA · On-site

Demonstrate sound editorial judgment, strong ethics, and unwavering journalistic integrity ... Ability to work varied shifts, including nights, weekends, and holidays as needed * Valid driver ...

Hearst

Investigative Reporter/Producer

Pittsburgh, PA · On-site

Demonstrate sound editorial judgment, strong ethics, and unwavering journalistic integrity ... Ability to work varied shifts, including nights, weekends, and holidays as needed * Valid driver ...

Hearst

Investigative Reporter/Producer

Pittsburgh, PA · On-site

Demonstrate sound editorial judgment, strong ethics, and unwavering journalistic integrity ... Ability to work varied shifts, including nights, weekends, and holidays as needed * Valid driver ...

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How much do weekend ethics investigator jobs pay per year?

As of Aug 6, 2026, the average yearly pay for weekend ethics investigator in the United States is $75,325.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $98,500.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Ethics Investigator jobs? The most popular types of Ethics Investigator jobs are:
Weekend Ethics Investigator jobs near you

Geriatrician - Principal Investigator

Pinnacle Clinical Research, LLC

Ridgewood, NJ

Full-time

Re-posted 10 days ago

Job description

Come join our team and make a difference as we blaze the way into the future of medical discovery through world-class clinical research. At Pinnacle Clinical Research, we are committed to driving innovation and advancing medical knowledge. Through our rigorous research studies, we strive to unlock breakthroughs that have the potential to transform patient care and improve lives. We pride ourselves on conducting high-quality research as a complement to the medical care that our volunteers receive from their routine care center. Together, we will raise awareness about the importance of clinical research and its role in shaping the future of healthcare. Be a part of the discovery!
Summary: Pinnacle Clinical Research is seeking a Full-time Geriatrician to serve as a Principal Investigator (PI) for clinical trials. The PI will oversee and conduct research activities, ensuring compliance with protocols, regulations, and ethical guidelines. Responsibilities include providing clinical oversight, monitoring patient safety, and collaborating with research staff to advance clinical studies. Ideal candidates will have significant experience in caring for patients with Alzheimer’s dementia and steatotic liver disease with strong analytical skills, and a dedication to advancing clinical research through high-quality patient care and ethical study practices.
The PI agrees to assume the overall responsibility for the study's conduct. By doing so, the User inherently agrees to:
• Personally conduct or supervise the research
• Ensure that each individual to whom a task is delegated is qualified by education, training, and experience to perform each of their delegated tasks
• Protect the rights, safety, and welfare of the participants who will be in their care. To do this, they agree that the research:
o Is conducted in accordance with all federal regulatory requirements, state law, and Pinnacle Clinical Research policies (including SOPs)
o Is conducted in accordance with the IRB-approved plan
o They will ensure the accuracy, security, and integrity of the research data and the subsequent analysis of that data.
Duties and Responsibilities:
• Review and hold expert knowledge of study-related activities and protocols.
• Assume all responsibilities and obligations as an Investigator, per Title 21 part 312 and FDA Form 1572.
• Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times.
• Maintain study sponsor and clinical trial confidentiality.
• Perform study-related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments. Review and adjudicate all lab, imaging, and biopsy findings.
• Assists in the preparation for study monitor visits.
• Perform subject screening and recruitment.
• Provide some weekend coverage to facilitate study visits by protocol.
• Provides after-hours phone call coverage as needed.
Qualifications:
• At least one to two years of clinical practice in Geriatrics
• Experience working with an aging population in a clinical or research setting
• Clinical research experience is preferred but not required
Knowledge, Skills, and Other Abilities:
• Bilingual (English and Spanish) strongly preferred
• Possess impeccable integrity and personal and professional values that are consistent with PCR’s high standards and mission
• Comply with the company policies, code of ethics, and guiding values always
Competencies:
• Must be able to work independently and collaborate with a team
• Excellent written and oral communication skills
• Organizational skills
• Ability to pay attention to detail
• People skills, including possessing a positive, friendly, and professional demeanor
• Ability to be flexible with changing priorities
• Ability to communicate in a diplomatic and professional manner
• Strong interpersonal skills
• Excellent computer skills
• Knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Foxfire, and web-based enterprise solutions software.
Certificates and Licenses:
• Current physician license.
• Board Certified in Geriatric medicine.
FLSA Classification: This is an exempt position.
Work Environment and Physical Demands:
The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
• Work may be performed in an office/laboratory and/or a clinical environment.
• Occasional travel may be required, domestic and/or international 10%.
• Ability to work in an upright and/or stationary position for 6-10 hours per day.
• Frequent mobility is required.
• Occasionally squatting, kneeling, or bending.
• Light to moderate lifting and carrying (or otherwise moving) objects, including medical equipment, with a maximum lift of 20-50 lbs.
Pinnacle Clinical Research is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.

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