Clinical Investigator

SGS•Richardson, TX

About The Position

We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. 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.

Requirements

Must possess a PhD, MS., or similar post-graduate degree in Science, Medicine, or Engineering
7+ years of experience in a related field
Ability to maintain confidentiality
Must be able to effectively work and manipulate large data sets.
Experienced user in Excel and the ability to learn and adapt with various software platforms
Effective communication, written and verbal skills
Strong attention to detail
Well organized with a sense of responsibility for project and time management
Ability to work in a fast-paced environment
Strong ability to balance multiple priorities and produce results
Excellent communication skills (verbal, written and presentation)

Nice To Haves

Dermatology background, sunscreen and cosmetic testing experience a plus
10+ years of experience in a related field is preferred

Responsibilities

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.
Handles any unanticipated occurrences on a case-by-case basis.
Notifies the Sponsor and the IRB about Adverse Events (AEs), Serious Adverse Events (SAEs) and Adverse Reactions (ARs).
Follows events and reactions to resolution.
Maintains Quality Assurance (QA).
Ensures that QA Department is fulfilling all job duties.