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Dear__________________:

I am seeking a challenging [ Insert Job Title ] role, and am submitting my resume for your review.

I am excited to build a rewarding career with your company, and can offer cross-functional experience in Clinical Research, Strategic Analysis / Planning, Team Building / Training, Regulatory Compliance, Nursing, Healthcare Operations, Treatment Planning, and Client Relations. I am also well-versed in Good Clinical Practices (GCP), International Conference on Harmonization (ICH) Guidelines, Nursing, Healthcare Operations, Treatment Planning, Records Management, Time Management, and Work Prioritization, among other areas. I have attained commendable achievements across a current workload of three protocols and two therapeutic areas (Cardiovascular Phase II / III; Pain Phase III) with 11 sites.

To complement my background, please note that I hold a Bachelor of Science in Nursing from Sojourner Douglass College and a Bachelor of Science from the University of Dschang in Cameroon.

As a Clinical Research Associate II for Clintriad Pharma Services, I expertly lead forward-thinking site selection, initiation, monitoring, and close-out visits in accordance with contracted scope of work and Good Clinical Practices (GCP), including comprehensively monitoring visits and site management for wide-ranging protocols, sites, and therapeutic areas to meet objectives. Within this role, I successfully administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues, including evaluating quality and integrity of study site practices related to proper conduct of protocols and adherence to applicable regulations. Furthermore, I proactively escalate quality issues to Clinical Project Manager (CPM), Clinical Research Specialist (CRS), and / or the line manager to ensure seamless operational processes at all times.

A sampling of my achievements include:

  Managing the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completions and submissions, and data query generation and resolution.

  Motivating investigators to achieve recruitment targets, and communicating efforts with Clinical Trial Manager.

  Ensuring the correct storage of drugs and the diligent account of all drugs in accordance with the sponsors SOP.

  Creating and maintaining documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, and generating detailed follow-up letters and other documentation.

[ Suggestion! Address Here Any Skills / Qualifications / Achievements Relevant to the Job Posting ]. As this is just an example of my abilities, please kindly refer to my enclosed resume for additional experience.

I look forward to hearing from you, and thank you in advance for your careful consideration.

Sincerely,

Delphine N. Forteh-Ngochi, BSN, RN