Research Coordinator Clinical Research Cover Letter

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

In my previous role, I was responsible for input into research protocol selection and coordinates study related communications with Research Team, patients, FH departments and customers (Sponsors, Clinical Research Organizations {CRO} and Study Monitors) in clinical research.

Please consider my experience and qualifications for this position:

• HS graduation (or GED) and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
• Willing to travel locally to off-site recruitment locations
• Willing to work some evenings and weekends in order to reach study participants (by telephone)
• Familiarity with rheumatic/autoimmune diseases, including rheumatoid arthritis
• Proficiency with Microsoft Office, including Word, Access, and Excel
• Demonstrated knowledge of medical and research terminology and familiarity in cardiovascular disease and its pathway
• Demonstration of commitment to CVC Core Values
• Previous experience in laboratory setting with laboratory policies and procedures

I am excited to be applying for the position of research coordinator clinical research. Please accept this letter and the attached resume as my interest in this position.

In the previous role, I was responsible for full range of research support (establish study procedures, develop project materials, coordinate and study protocol, recruit and enroll subjects, operate the study device and related equipment, collect and record data, assist with regulatory compliance, and assist with data analysis).

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

• Knowledge and experience in budgeting, accounting and contracting is preferred
• Self-motivated individual able to manage multiple tasks and priorities in an efficient manner
• Can work independently without direct supervision in a team environment
• Experience working in a clinical research lab (e.g., exposure to human subjects IRB protocols, interaction with research participants)
• Knowledge of psychological test psychometrics
• Previous experience conducting independent data analysis
• Familiarity with statistical software (e.g., R, MPlus, SAS, SPSS)
• Familiarity with online data collection systems (e.g., Qualtrics)

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

In the previous role, I was responsible for input and guidance on clinical research study management and clinical research policies and procedures.

Please consider my qualifications and experience:

• Familiarity with and strong interest in statistical programs such as R, SAS, Stata, SPSS
• Experience with electronic medical records or Medicare claims data
• Basic fluency in Microsoft Office (Word, Excel, PowerPoint, & Outlook), use of mobile telephones (e.g., sending/receiving text messages including photographs, mobile security, ), and use of video conferencing tools (e.g., Skype, FaceTime)
• Creation of campaigns and ads within Facebook, Twitter, Instagram, and Grindr
• Experience with recruitment and retention of this participant population (i.e., individuals living with HIV)
• A registered nurse (RN) licensure
• Internship or prior work experience in clinical research at a hospital, CRO, or biopharmaceutical company is strong preferred
• Medical terminology, knowledge of disease processes and anatomy, oncology

I am excited to be applying for the position of research coordinator clinical research. Please accept this letter and the attached resume as my interest in this position.

In my previous role, I was responsible for leadership in complex clinical research activities including: reaching agreement on study goals with other functional areas, coordinating and overseeing study monitors and investigators to ensure compliance, monitoring, analyzing and interpreting study data, and preparing reports.

Please consider my qualifications and experience:

• Experience with clinical research coordination
• Experience working with transgender patients and their families/caregivers
• Fluency in the usage of Committee of Human Research (CHR) online iMEDris system or another IRB system
• Requires experience in creating database and financial analysis
• Experience with data collection and database maintenance
• Knowledge of clinical research techniques
• GCP, HIPAA, CHR and other CRC related training
• Knowledge of basic science research techniques

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

In my previous role, I was responsible for full spectrum of study coordination services to principal investigator clients and their research teams, including study preparation for coordination, participant screening and recruitment activities, scheduling and coordinating study visits, interacting with research participants, collecting and submitting study data, processing, handling and shipping research samples, coordinating sponsor monitoring visits, etc.

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 with electronic medical records and administering health screening questionnaires
• Experience with internet database entry
• Experience with biological sample processing
• Experience with performing spirometry
• Experience in patient recruitment and follow-up for clinical research studies
• Experience in developing, maintaining, and following clinical research protocols, obtaining consent and follow-up in an urban setting with diverse patient demographics and cultures
• Experience in data collection and data management in clinical research setting
• Experience with the REDCap database system