Clinical Trials Assistant Cover Letter

Please consider me for the clinical trials assistant opportunity. I am including my resume that lists my qualifications and experience.

In my previous role, I was responsible for an ongoing annual professional contribution: Ensures research documentation is comprehensive and facilitates protocol compliance; communication among colleagues; good clinical research practice; and patient safety.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• Excellent grasp of English language, medical terminology
• Demonstrated aptitude for working in a highly regulated field with adherence to quality standards
• Assist in the development of standard operating procedures for study protocols
• Assist in the development of study forms, necessary database programs & data collection/entry strategies with applicable staff
• Assist with recruitment, coordination of care (in compliance with study protocol), and retention of research subjects
• Complete study activities as dictated by research protocols
• Maintain a current clinical trial listing of all studies managed by Neuro-Oncology Research for the purposes of informing physicians/staff and potential subjects (via NorthShore website) of available research studies
• Ensure that study documents are complete, current, and filed correctly

In response to your job posting for clinical trials assistant, I am including this letter and my resume for your review.

In my previous role, I was responsible for management oversight, mentoring, training and guidance to drive process efficiency and excellence to support clinical studies and business initiatives in accordance with good clinical practice, corporate procedures and relevant regulations and laws.

Please consider my qualifications and experience:

• Participating in planning, initiation, and reporting activities of clinical trials according to company procedures and international regulations
• Act as local subject matter expert/key user for BI systems and processes
• Participate in global and local initiatives aimed at increasing quality and delivery of clinical operations activities
• Six to 12 months prior experience
• Working knowledge of computers (either DOS-based or Macintosh)
• Standard office software packages (Word, WordPerfect, Lotus, Excel, Access, Power Point)
• Standard office equipment (photocopiers, facsimiles, telephones, pagers)
• Familiar with medical, scientific or healthcare environments either through coursework or experience

I would like to submit my application for the clinical trials assistant opening. Please accept this letter and the attached resume.

In the previous role, I was responsible for guidance on DF/HCC training requirements and instructions on how to access and complete including Human Subject Protection Training, Good Clinical Practice Training and DF/HCC SOP Certification.

My experience is an excellent fit for the list of requirements in this job:

• Certified Nursing Assistant, Emergency Medical Technician, Medical Asst Diploma or Certification
• CTA experience is preferred
• Excellent computer, telephone and customer service skills
• Proficient in using Microsoft Word
• CPR validated within 3 months of hire
• Certification as CNA
• Interest in oncology and clinical research
• Human subject research experience

In response to your job posting for clinical trials assistant, I am including this letter and my resume for your review.

In my previous role, I was responsible for technical support and training to clinical investigators and their staff in regards to device trial information, the protocol, clinical and regulatory requirements and device implant support.

My experience is an excellent fit for the list of requirements in this job:

• Fluency working with electronic spreadsheets (Microsoft Excel)
• Experience leading research professionals
• Current certification as a clinical research coordinator (CCRP®, CRC®, CRA®) or other applicable clinical research certification
• Demonstrated experience handling biological samples (blood and urine specimens)
• Strong experience using Microsoft Word, WordPerfect, and Excel and data entry experience
• Knowledge of FDA regulations, Good Clinical Practices, and ICH Guidelines
• A strong academic record, excellent problem-solving abilities, exceptional communication skills, strong quantitative skills, and be a proven team contributor
• Manage and support the essential document management process according to Good Documentation Practice and the Trial Master File SOP

I submit this application to express my sincere interest in the clinical trials assistant position.

In my previous role, I was responsible for guidance on good clinical research practice in developing research sites.

Please consider my experience and qualifications for this position:

• Experience with word processing, spreadsheet organization and manipulation is preferred
• A professional level of knowledge or psychological and/or biological research and familiarity with scientific terminology
• Requires a working knowledge of statistics, computer applications and research methodologies
• Proficiency using Microsoft Word, WordPerfect, and Excel and data entry experience
• Background working in research or a medical setting preferred
• Medical terminology experience or familiarity preferred
• Knowledge of human growth and development to modify care to age and developmental stage of the patient
• Physically able to perform the tasks of the role, such as walking, standing, pushing, and bending