Clinical Research Assistant II (Contract) - On Call - 6-8 weeks

SGS; Richardson (TX); On-site; USD 30,307 - 38,572; Full time

Job summary

SGS is seeking a Clinical Research Assistant II (Contract) on call for 6-8 weeks in Richardson, TX. You will support study procedures in the clinic and perform related administrative duties to assist coordinators, following GCP guidelines and SOPs.

Responsibilities include ESAQ administration, informed consent handling, materials QC, and preparation of study documents while delivering strong customer service and precise coordination across multiple projects.

Qualifications

• Associates degree or at least one year of administrative/clerical work experience.
• Strong attention to detail and organizational, verbal and written communication and interpersonal skills.
• Able to follow instructions and study protocols according to GCP guidelines, applicable regulations, and SOPs.

Responsibilities

• Performs daily clinic tasks to assist coordinators with study procedures, including ESAQ administrations, check-in, informed consent signing, instrumentation and photography assistance.
• Performs daily administrative tasks to assist coordinators in study preparation and conduct, including test material preparation, appointment reminders, and QC of study documents.
• Assists in the development of study paperwork for coordinators.
• Reports to clinic on time for all studies assigned to work.
• Performs tasks according to GCP guidelines, applicable regulations, SOPs and work instructions.
• May perform tasks for other departments as needed.
• Provides excellent customer service to clients and panelists, maintaining positive interactions with peers and leadership.
• Complies with safety and Operational Integrity procedures and processes.

Skills

Attention to detail

Verbal and written communication

Organizational skills

Education

Associates degree

Job description

Clinical Research Assistant II (Contract) - On Call - 6-8 weeks

This is a Contract 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.

Responsibilities

• Performs daily clinic tasks to assist coordinators with study procedures, including Electronic Self-Assessment Questionnaire (ESAQ) administrations, check-in process, informed consent signing, instrumentation assist, photography assist, etc.
• Performs daily administrative tasks to assist coordinators in study preparation and conduct, including test material preparation, making appointment reminders, quality checking (QC) study documents, etc.
• Assists in the development of study paperwork for coordinators.
• Reports to clinic on time for all studies assigned to work.
• Performs tasks according to Good Clinical Practice (GCP) guidelines, applicable regulations, standard operation procedures (SOP), and work instructions.
• May perform tasks for other departments as needed.
• Provides excellent customer service to clients and panelists, and maintains positive and respectful interaction with peers and leadership.
• Complies with and understands safety and Operational Integrity procedures and processes.

Qualifications

• Associates degree or at least one year of administrative/clerical work experience.
• Strong attention to detail and organizational, verbal and written communication and interpersonal skills.
• Able to follow instructions and study protocols according to GCP guidelines, applicable regulations, and SOPs.
• Able to lift moderately heavy items.
• Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.
• Must be flexible to work morning/afternoon shifts.

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 be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.

This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.