Clinical Research Cover Letter

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

In my previous role, I was responsible for guidance and support to the research community regarding the registration and reporting requirements for all clinical research.

Please consider my experience and qualifications for this position:

• Proven track record of successful projects (delivered on time, within budget, and with high quality)
• BS or MS in chemistry, biochemistry and chemical engineering
• Experienced with protein purification ( small and large scale)
• Bench work, organic chemistry (synthesis) and/or protein isolation, purification
• Mobility in the national territory
• Knowledge of the e-system EDC, IMPACT, IVWRS and Clinphone
• Highly motivated and be able to work with minimal supervision
• BOC certified athletic trainer and eligible for Florida AT license

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

In my previous role, I was responsible for collaborative leadership and management oversight and coordination of special research projects for the NIAID, Division of Clinical Research (DCR), Office of Planning and Operations Support (OPOS).

Please consider my experience and qualifications for this position:

• Consistently meet or exceed agreed quality metrics
• May act as mentor, lead CRA, therapy area lead/compound for project teams
• Experience in UK clinical trial site management of Oncology Phases I to IV
• Experience in collaborations with relevant trade organizations, hospitals and physicians
• Bachelors's or master's equivalent experience with mammalian cell culture, bench scale Bioreactor operations
• English proficiency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system
• Experience in managing clinical research data collection, reporting, outcomes, quality improvement, and standards/pathways
• Experience in meeting (CFR, GCP, ICH, OHRP guidelines), other Federal, State and Local regulations surrounding human research and gene therapy practices

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

In the previous role, I was responsible for routine information and advice to research staff, administrators, and service area managers regarding clinical research budget and billing policies and activities; and serve as liaison between CRBB and partners in clinical research.

Please consider my qualifications and experience:

• Experience with patients and/or medical research
• Demonstrate positive interpersonal skills, especially when interacting with other medical professionals including nurses, respiratory therapists, physicians, and paramedics
• Able to adhere to specific protocols for all data collection
• Maintain exceptional attention to detail
• Demonstrate computer proficiency with knowledge and experience with word processing, spreadsheet and presentation software, such as Microsoft Excel, Word and PowerPoint
• Research experience, particularly in a school setting
• At least three months of experience in medical research
• Proficiency in data management using Excel, Access, or a similar database

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

In my previous role, I was responsible for clarification and direction to post award analysts regarding the budget, invoicing and financial management of clinical research funds.

Please consider my qualifications and experience:

• Execute total site management including evaluation, initiation, monitoring visits, regulatory assessment, drug supply management and resolution of issues to ensure compliance and that site activities are in line with milestones
• Participate to trial site training activities as assigned
• Demonstrate and apply GCP and ICH requirements
• Ensure site level update of technical systems such as ClinAdmin and authoring study monitoring reports in accordance with timelines
• Perform monitoring visits according to the monitoring plan as assigned, including source document verification
• Drive and assist with data query resolution process both at site and with Data Management
• Manage protocol and process deviations according to SOPs
• Perform site closeout activities

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

Previously, I was responsible for training to the Clinical Research Management Office (CRMO) teams, Data Managers, and Nurse/Coordinators on kit preparation.

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

• Prior experience with patients and patient interaction
• Has a broad understanding of applicable related regulations and ICH GCP requirements
• Positive and a proactive approach to identification and definition of problems, and with the development and implementation of solutions
• Demonstrate diplomacy and tact while maintaining appropriate assertiveness and persistence
• Certification in clinical research coordination (SoCRA, ACRP)
• Clinical research experience, oncology clinical research experience
• Understanding of GCP, ICH, and HIPAA regulations
• Familiarity with the code of federal regulations governing clinical research