PhD, M.D., D.O., or similar post-graduate degree in Science, Medicine, or Engineering required.
7+ years of experience in clinical research or a related field.
Dermatology background and experience in sunscreen and cosmetic testing preferred.
10+ years of experience in a related field is a plus.
Strong project management skills in a fast-paced environment.
Responsibilities
Oversee clinical research involving healthy paid volunteers.
Write protocols, collect and review data, and prepare progress reports.
Develop and maintain Standard Operating Procedures (SOPs) for clinical research.
Conduct and supervise studies in accordance with protocols and SOPs.
Protect the rights, safety, and welfare of study subjects.
Interface with sponsors, IRBs, and other stakeholders to obtain necessary documentation.
Notify sponsors and IRBs of any protocol changes or deviations.
Benefits
Medical, dental, and vision insurance, along with life insurance and employee assistance programs.
401(k) plan with company match and immediate vesting upon enrollment.
Access to online training courses and tuition reimbursement for professional growth.
Paid time off and family leave to support work-life balance.
Full Job Description
Job Description
The 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.
Qualifications
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.
Additional Information
Salary: $90,000 - $120,000 USD
Our Benefits
We care about your total well-being and will support you with the following, subject to your location and role.
Health: Medical, dental and vision insurance, life insurance, employee assistance programs.
Wealth: In addition to base pay, we offer 401(k) with company match (immediate vesting upon enrollment).
Happiness:
Professional Growth: Online training courses, virtual and classroom development experiences, tuition reimbursement program
