DATA/MEDICAL INVESTIGATOR (Ridgewood) Job at Pinnacle Clinical Research, Ridgewood, NJ

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  • Pinnacle Clinical Research
  • Ridgewood, NJ

Job Description

Pinnacle Clinical Research Job Description
Principal Investigator
Reports To: Medical Director
Investigators
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. 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.
Ensure that each individual to whom a task is delegated is qualified by education, training, and experience to perform each of their delegated tasks
Is conducted in accordance with all federal regulatory requirements, state law, and Pinnacle Clinical Research policies (including SOPs)
They will ensure the accuracy, security, and integrity of the research data and the subsequent analysis of that data.

Assume all responsibilities and obligations as an Investigator, per Title 21 part 312 and FDA Form 1572.
Provide some weekend coverage to facilitate study visits by protocol.
Provides after-hours phone call coverage as needed.
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
Ability to be flexible with changing priorities
Excellent computer skills
Knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Foxfire, and web-based enterprise solutions software.
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%.
Light to moderate lifting and carrying (or otherwise moving) objects, including medical equipment, with a maximum lift of 20-50 lbs.
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.

Job Tags

Full time, Part time, Work at office, Local area, Flexible hours, Weekend work,

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