Clinical Research Assistant

ADP, Inc.; Corpus Christi (TX); Sur place; USD 38 000 - 46 000; Plein temps

Avantages offerts par ce poste

401k

Medical, dental, vision

Disability insurance

FSA

Life insurance

3 weeks paid time off

14 holidays

Résumé du poste

Summit Clinical Research Solutions in Corpus Christi, TX is seeking a Clinical Research Assistant to support the Clinical Operations team. You will assist with study documents, regulatory submissions, sponsor liaison, and site visits to help keep trials on track.

Responsibilities include maintaining CTMS data, coordinating with physicians and nurses, and supporting patient assessments and recruitment under SOPs and FDA/ICH GCP guidelines.

Qualifications

• High school diploma or GED; or 2–4 years related experience and/or training; or equivalent combination.

Responsabilités

• Assist with creation and completion of study documents and preparation.
• Help with regulatory submissions and file maintenance.
• Serve as secondary liaison with sponsors.
• Prepare for study monitor visits as directed.
• Create reports as requested.
• Complete study assessments with patients, including AEs and vital signs.
• Assist with subject screening and recruitment as directed.
• Update CTMS as directed.
• Coordinate multiple projects with competing priorities.

Connaissances

Oral comms

Written comms

Organization

Attention to detail

Flexibility

Medical terminology

Microsoft Office

CTMS knowledge

Formation

GED/High school diploma

Clinical research certification preferred

Outils

CTMS

ECRF systems

Office suite

Description du poste

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Clinical Research Assistant

Clinical Operations CCTX Full Time Corpus Christi, TX, US

Summary: Assists the Clinical Research Coordinator and the principal investigator with administering activities to facilitate clinical research, which may include working with an affiliate or collaborating research sites. Exercises judgment within the allowable limits defined within clinical trials protocols, standard operating procedures, and under the direction from the study Investigator and supervisor. Always maintains subject and document confidentiality, understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards (IRB), and institutional policies and procedures by performing the following duties.

Duties and Responsibilities:

• Assists with the creation and completion of study related documents and new study preparation.
• Assists with the completion of regulatory submissions and maintains regulatory files as directed.
• Acts as a secondary liaison with sponsors.
• Assists with the preparation for study monitor visits as directed.
• Creates reports as requested.
• Completes study directed assessments with patients to include, but not limited to adverse events, test article (TA) handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessment.
• Assists with subject screening and recruitment as directed.
• Updates Clinical Trial Management Software (CTMS) as directed.
• Coordinates multiple projects with competing priorities and deadlines, as needed based on clinical trial protocol directives and study volume.
• Interacts with internal and external personnel to include, but not limited to physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel, and clinical trial patients.

Education/Experience:

High school diploma or general education degree (GED); or two to four years related experience and/or training; or equivalent combination of education and experience.

Certificates and Licenses:

• Clinical research certification preferred

Knowledge, Skills, and Other Abilities:

• Ability to demonstrate competence in oral and written communication
• Must be organized, attentive to detail, and possess a positive, friendly, and professional demeanor
• Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
• Medical knowledge, including medical terminology
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.
• Must have knowledge of Microsoft Office Word, Microsoft Excel, Internet Explorer, Google Chrome, Mozilla Firefox, web-based enterprise solutions, and Electronic Case Report Form systems.

Work Environment and Physical demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Work is performed in an office/laboratory and/or a clinical environment.
• Exposure to biological fluids and/or bloodborne pathogens.
• Personal protective equipment required such as protective eyewear, garments, and gloves.
• Occasional travel may be required domestic and/or international.
• Ability to work in an upright and/or stationary position for 6-10 hours per day.
• Frequent mobility required.
• Occasional squatting, kneeling, or bending.
• Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.

Perks of working at Summit Clinical Research Solutions:

• 401k
• Medical, dental, vision, long term disability, short term disability, FSA, and life insurance
• 3 weeks of paid time off
• 14 paid company holidays
• Scrub voucher (specific positions apply)
• And more!

Summit Clinical Research Solutions is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.