Clinical Research Coord Cover Letter

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

Previously, I was responsible for guidance and direction to staff engaged in clinical research or trials to ensure compliance with protocols and overall clinical objectives.

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:

• Technical set-up, hands-on equipment responsibilities, and data acquisition for research studies
• Data analysis, EEG and physiological time series
• Software development and code management
• Collect and maintain subject information database (SQL) for studies
• Assist in data collection, analysis, and report generation
• Comply with HIPPA regulations and patient confidentiality
• Write, produce and maintain all Institutional Review Board (IRB) documentation for study protocols
• Experience with electrical engineering or a related field is strongly preferred

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

In my previous role, I was responsible for multifaceted support to the Clinical Research Department in areas of project coordination, data management and analysis, communication and administrative assistance for Abbott Northwestern Hospital Foundation funded research study.

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:

• Should be comfortable doing a variety of tasks, be able to balance multiple commitments, and be proficient at adaptive multi-tasking
• Should demonstrate interest in the work, a strong work ethic, and personal and professional integrity
• Outstanding interpersonal, communication, and organizational skills are essential
• Energetic, interactive and comfortable working independently and also as part of a team
• Effectively communicates with investigators, coordinators, and co-workers
• Has strong computer skills as evidenced by proficient knowledge of Microsoft office tools (e.g., word, Excel, power point)
• Experience with EPIC and RedCap preferred
• Phlebotomy expertise preferred

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

In the previous role, I was responsible for subject matter expertise in medicine for all clinical research studies during the design and implementation phases of study protocols.

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

• Experience using basic computer programs including word processing, database, spreadsheet applications and e-mail
• Experience using laboratory protocol, systems and documentation techniques
• Track enrollment status of subjects, ensure coordination of care from inpatient to outpatient, and at times follow up after discharge
• Ensure consent is obtained properly prior to sample collection
• Establish and maintain relationships with hospital staff
• Direct the collection, labeling, storage, or shipment of research specimens
• Manage the Severe Immunotherapy Complications (SIC) database
• Confer with investigators and input data regarding adverse events into the SIC RedCap database using source documentation in the EPIC chart

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

In my previous role, I was responsible for education for the staff, patients and their families regarding research protocols, study medications and clinical procedures.

Please consider my experience and qualifications for this position:

• Experienced in the use of MS Office software, including word processing
• SOCRA or ACRP certification
• Exposure to clinical trials or related health field
• Working knowledge of FDA, NIH and OHRP regulatory requirements and ICH GCP guidelines
• Oversee workflow of others and distribute tasks
• MPH optional
• Pre-med track” optional
• Excellent command of English including medical and technical terms

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

In my previous role, I was responsible for guidance, direction and oversight in the development of SOP’s, protocols, documentation standards etc., for use in the preparation of clinical trial and research study budgets.

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

• Demonstrated knowledge of signs, symptoms, pathology of HIV infection, Hepatitis B & C infection and STI's
• Demonstrated experience performing HIV testing and counseling
• Experience interpreting laboratory values to determine subject’s eligibility and potential toxicities and insight to know when abnormalities should be reported to a clinical nurse or Physician
• Proficient with Microsoft Office Suite and electronic database management
• Phlebotomy trained/certified
• Updates binders
• Acts as study resource for sites
• Reviews work of trainees