Live opening · Posted 5 days ago

Junior Clinical Investigator

SGS · Phoenix, AZ, United States
Smartrecruiters No Full-time
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At a glance

The key details from the original listing.

Posted 5 days ago
CompanySGS
LocationPhoenix, AZ, United States
Job typeFull-time
Work modeNo
SourceSmartrecruiters
Listed5 days ago

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About the role

Description supplied by the original job listing.

The Jr. Clinical Investigator, CRS oversees the clinical research of consumer products involving healthy paid volunteers. Develops research studies and creates standards and guidelines for clinical research services and programs. Ensures adherence to standard operating procedures, good clinical practice and FDA regulations.
Oversees the clinical research of consumer products involving healthy paid volunteers.
Writes protocols, collects and reviews data, prepares progress reports, analyzes results, writes summaries and conclusions and issues reports.
Develops, maintains and reviews Standard Operating Procedures (SOPs). Ensures that study personnel have access to SOPs and that SOPs are followed.
Conducts and / or supervises studies in accordance with the protocol and SOP’s.
Protects the rights, safety and welfare of subjects.
Interfaces with the Sponsor, staff, contractors, professional societies, Institutional / Investigational Review Board (IRB), subjects, government agents / agencies and other business units. Obtains appropriate information, documentation and signatures.
Notifies the Sponsor and / or IRB of any changes to or deviations from the protocol and document changes and deviations.
Delegates duties, as appropriate. Ensures that all individuals working on the study have necessary credentials, are adequately trained, understand their obligations and are properly supervised.
Provides a sufficient number of trained staff members to be assigned to each study. Maintains training records of staff members.
Ensures that the Informed Consent (IC) is clear and accurate so that subjects can understand the IC. Provides the opportunity for subjects to ask questions about the IC. Ensures that subjects have signed the IC.
Must possess a PhD, M.D., D.O., or similar post-graduate degree in Science, Medicine, or Engineering
7+ years of experience in a related field
Dermatology background, sunscreen and cosmetic testing experience a plus
10+ years of experience in a related field
Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.

Employment type
Full-time

Work arrangement
No

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