Clinical Research Supervisor at SGS North America Inc. in Richardson, Texas

Job Description:

Company Description




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 97,000 employees operate a network of 2,650 offices and laboratories, working together to enable a better, safer and more interconnected world.




Job Description

• Understands requirements for all studies and communicates same to all personnel/departments involved in each study.


• Supports, advises, and mentors new clinic staff.


• Conducts training on new procedures related to research studies.


• Provides feedback to employees and recommend reprimanding when necessary.


• Oversees study conduct, including supervision of clinic staff, study flow, timekeeping, coordinating subjects to appropriate steps/location, checking in with grader on any specific requests and communicating with recruiting.


• Ensures that clinic is properly set up for the day's studies.


• Assist in clinic staff scheduling.


• Ensures inventory of internal supplies needed for studies is at a level to support current and upcoming studies.


• Approves study supply requests after verifying supplies are not in stock, they are appropriate for study needs and are ordered in a timely manner.


• Reviews and approved various documents relating to each study.


• Performs verification and approval of Test Handling & Preparation Form.


• Handles panelist questions and concerns that cannot be handled by staff.


• Explores and implements ways to improve clinic operations, SOPs and/or training materials.


• Provides manager and Investigators with routine updates on the clinic operations and staff.


• Other duties or tasks assigned by manager.

PHYSICAL DEMANDS OF THE JOB

• Stand Occasionally


• Move or traverse Occasionally


• Sit Frequently


• Use hands Frequently


• Reach with hands and arms Occasionally


• Climb or balance None


• Stoop, kneel, crouch or crawl None


• Talk/hear Frequently


• Taste/Smell None


• Lift/carry/push or pull Occasionally 20 lbs

Qualifications

• Bachelor's degree - preferably in science Required


• Minimum 2 or more years Clinical Research Coordinator experience Required

LICENSES / CERTIFICATIONS

• CCRC/CCRA certification Preferred

KNOWLEDGE / SKILLS / ABILITIES

• Strong organizational, communication and interpersonal skills


• Demonstrated multi-tasking skills


• Strong decision-making/analytical skills


• Proficiency with Microsoft Office applications


• Knowledge of GCP/CLP guidelines and Federal Regulations related to the conduct of clinical trials, NIH training and CCRC/CCRA certification a strong plus


• Ability to maintain confidentiality.


• Strong attention to detail.


• Well organized with a sense of responsibility for project and time management.


• Ability to handle multiple competing priorities through effective resource management.


• Mathematical Skills: Intermediate preferred.


• Reasoning Skills / Abilities: Intermediate preferred.


• Computer Skills: Intermediate preferred in Microsoft Office Suite

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