Clinical Research Coordinator jobs in Albany, NY

EEO

Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.

IMA Clinical Research is looking for a Neurologist (MD or DO) who is interested in working as a clinical investigator for pharmaceutical clinical research studies in our Albany New York medical office. IMA Clinical Research conducts outpatient research studies in all phases of drug clinical development (Phases 1b-4).

This is an exciting opportunity to work at the cutting edge of clinical drug development. Position may be a good fit for a Board-Certified Neurologist who has an interest in Clinical Trials.

Duties and Job Functions include but not limited to:

• Provide oversight and ensure proper delegation of duties to appropriate qualified staff.
• Provide Sponsor and IRB with documentation of credentials as required.
• Maintain all required licenses to practice and trainings required to execute the job as PI or Sub-I.
• Assume responsibility as the Principal or Sub-Investigator for the duration of clinical trials.
• Demonstrate the proper education, training and experience to conduct the clinical investigation.
• Disclose conflicts of interest as described in the regulations.
• Evaluate and screen potential subjects based on study eligibility criteria.
• Perform and review assessments performed by raters in accordance with the clinical study protocol.
• Complete all documentation, paper and electronic, as required per protocol.
• 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 and educational seminars.
• Travel to Investigator meetings as needed.
• Diversity and bi-lingual capabilities are desirable.

Requirements:

• MD or DO
• Active Medical License
• Previous Experience as a Principal Investigator or sub-investigator is desirable but no required.

Benefits:

• Competitive Salary starting at $135,000 and Benefits.