Clinical Research Coordinator Cover Letter

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

In my previous role, I was responsible for assistance to physicians analyzing images in the clinical trials (imaging data transfer and upload, preparation of image reading sessions, collection of data forms, transfer of data into electronic database).

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:

• Experience in clinical pulmonology and clinical/epidemiology/pulmonary research
• Proficiency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system
• Demonstrated familiarity with maternal and child medical records and medical record abstractions
• Demonstrated experience with large data collection activities including comprehensive participant interviews
• Knowledge and demonstrated past research experience of child developmental disabilities including autism spectrum disorder
• Knowledge and demonstrated past research experience of maternal health in pregnancy, pregnancy exposures, and perinatal and neonatal health outcomes
• Sensitivity in communicating with vulnerable populations
• Experience with web-based computer applications and Microsoft Access databases

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

In the previous role, I was responsible for instruction on research protocols including interpretation of test results, observations, and related study data to physicians, nurses, professors, teachers, and technician involved.

Please consider my qualifications and experience:

• Experience with clinical trials, statistics and/or data management
• Knowledge of clinical research in gastrointestinal oncology
• Statistics background and experience working with statistical tools such as Access, SPSS and/or Stata
• Previous clinical trials experience (including knowledge of IRB policies and procedures)
• Previous experience with data entry under HIPAA standards and regulations
• BA or BS in biological sciences or related field, or RN or if an Intern a student in one of these areas
• Work experience in life science or medically related field
• Awareness and working knowledge of applicable clinical research regulatory requirements , good clinical practice (GCP) and International Conference on Harmonisation (ICH) guidelines preferred

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

Previously, I was responsible for input for the clinical database build, CRFs, monitoring plan, data management plan, and statistical analysis plan.

Please consider my experience and qualifications for this position:

• Familiarity with internal University processes and programs (MiChart, REDCap, eREearch)
• Proven data entry accuracy and efficiency
• Previous experience with biobank/biorepository
• Basic understanding of intervention study design
• Experience with a public health campaign or similar messaging targeting health behavior change
• Experience designing online advertisements for social media and other recruitment sources for research
• Smoking cessation treatment certification
• Knowledge of smoking cessation and depression treatment techniques

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

In the previous role, I was responsible for training and guidance to research and non-research personnel on becoming Collaborative Institutional Training Initiative (CITI) Program trained in Social Behavioral Sciences and Biomedical Sciences.

Please consider my experience and qualifications for this position:

• Nursing or similar background or
• BS/BA in biology or related field or
• Master’s level education in clinical research or public health
• Society of Clinical Research Associates (SOCRA) Certification
• Experience with research study budget preparation
• Experience with project coordination for multi-center trials
• Knowledge of HIPAA compliance guidelines
• Experience working with patients under the age of 18

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

In my previous role, I was responsible for clinical Science support for a growing cancer immunotherapy (CIT) program, primarily medical data review of ongoing CIT combination studies.

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:

• Develops a working knowledge of study regulations and billing processes
• Working knowledge of statistics, database management, and human subject research in a clinical setting
• Willingness to work weekends and evenings, as necessary
• Prior experience administering mental health or neurocognitive assessments
• Experience working in HIV and/or women’s health research
• Demonstrated knowledge of HIV-medications and medical terminology
• Experience with Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols
• Experience working in a clinical and/or research environment