Clinical Data Coordinator Cover Letter

I submit this application to express my sincere interest in the clinical data coordinator position.

Previously, I was responsible for general administrative support to Clinical Trials Office; helping manage research files and checklists, and entering data in to UNLV's clinical trials management system.

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:

• Unblinded SAS Programmer
• Electronic and paper medical records experience preferred
• Software applications experience, which includes Word Processing, Excel and Access preferred
• Research and statistics experience preferred
• Eligibility for SoCRA certification preferred (more information at SoCRA.org)
• LPNs and CMAs preferred
• Assists will all aspects of cardiopulmonary exercise testing, including metabolic cart calibration and preparation, blood gas and chemistry analyses, and data reporting
• Participates in research protocols spanning a large range of areas that primarily relate to applied human exercise physiology

I submit this application to express my sincere interest in the clinical data coordinator position.

In the previous role, I was responsible for strategic operational leadership in planning, prioritizing, executing and sourcing internal and external data management and/or clinical programming activities for multiple clinical trials.

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:

• Knowledge and experience with multiple software programs
• Knowledge and experience of Meditech clinical documentation system
• Knowledgeable of FDA requirements to ensure quality databases submissions and associated documentation
• Experience performing user acceptance testing of clinical study databases
• Experience designing electronic Case Report Forms (eCRFs) for study start-ups
• Experience in supporting medical device studies preferred
• Exposure to SAS preferred
• Willingness to obtain IATA/DOT certification prior to start date

I submit this application to express my sincere interest in the clinical data coordinator position.

In my previous role, I was responsible for data management and study coordination for clinical research trials (investigator initiated and commercially sponsored trials).

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:

• Actively participates in research database creation, upkeep, and analysis
• May assist with writing protocols and manuscripts for submission to research journals and national scientific meetings
• Experience in database design and management is preferred
• Maintains current knowledge of ACC data collection and/or reporting process changes to various definitions
• Spanish-speaking is strongly preferred
• Requires interpersonal skills necessary to coordinate research studies and interact with staff, physicians, and patients
• Proficiency in medical terminology (oncology)
• GCP and ICH

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

In the previous role, I was responsible for clinical data management leadership within the study team to align on and drive data collection requirements for one or more complex clinical development projects.

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:

• Oncology background preferred
• Experience using EMR and strong computer skills preferred
• A physical science or engineering background is preferred
• A physical science, life science or engineering background is preferred
• Comfortable with database query language (specifically SQL)
• Basic knowledge of Diabetes
• Knowledge of medical terminology, ICD-9 and CPT coding and DRGs
• Experience with statistical analysis and data display techniques

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

In the previous role, I was responsible for guidance to Clinical Data Managers working within assigned program and ensures operational consistency across assigned clinical trials.

Please consider my qualifications and experience:

• Demonstrate organizational and communication skills
• Demonstrate written, verbal, and interpersonal communication skills
• Demonstrate proficiency in medical terminology
• Demonstrate good prioritization and organizational skills
• Demonstrated skill in administrative tasks (i.e., filing, photocopying, faxing)
• Demonstrates expertise with subject matter
• Participation in community, state and professional organizations related to quality management and improvement
• Computer proficient including internet use and management of multiple databases