Junior Clinical Investigator

SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services.

Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.

• 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.

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.
• Work-Life Balance:
  Paid-time off and family leave.

SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.

To perform this job successfully, an individual must…