Medical Affairs Cover Letter

Please consider me for the medical affairs opportunity. I am including my resume that lists my qualifications and experience.

Previously, I was responsible for regulatory assistance and review of clinical study documentation, including review of clinical protocols, informed consent documents, and clinical study recruitment materials.

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:

• May have performed protocol design in the academic environment or in the pharmaceutical industry and/or acted as an assistant PI or PI
• Detailed, organized, and able to work independently
• Composes and types routine memos and correspondence at an executive level
• Copies, faxes and routes information as requested
• Responds to a broad range of inquiries
• Keeps management's calendar up-to-date
• Makes necessary arrangements to ensure details for meetings are completed
• Conducts outside research for projects, as necessary

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

Previously, I was responsible for strategic input and regulatory approval for clinical study protocols, including clinical protocols for EU investigator initiated studies, and protocol amendments.

Please consider my qualifications and experience:

• High quality standards, attention to detail, tenacious follow-up
• Has previously worked in an International environment over multiple time zones
• Experience supporting a Global Team
• Proven track record to diligently work in cross-functional teams
• Advanced computer skills (MS Excel, Word, Powerpoint)
• Excellent knowledge of budgeting process and accounting principles
• Project management skills, effectively manage multiple priorities
• Highly adaptive and flexible to high through-put business environment

I submit this application to express my sincere interest in the medical affairs position.

In my previous role, I was responsible for input into safety sections of study protocols, regulatory submissions, and clinical/regulatory reports, including clinical risk/benefit analysis as required.

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

• Prepares recurring and special reports and presentations by gathering data, interpreting data and assembling reports using PowerPoint, Excel, for executive's review and distribution
• Proofreads and edits materials
• Provides confidential administrative and clerical support to executive
• Receives, opens, sorts, reads and prioritizes executive's mail
• Schedules appointments, meetings, conferences, luncheons, hotel reservations and travel plans
• Serves as a receptionist for executive, receiving and screening visitors and telephone calls
• Serves as recording secretary for committee(s), scheduling meetings, distributing materials, recording and transcribing meeting minutes
• Build and maintain effective partnerships with Marketing counterparts

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

In my previous role, I was responsible for safety input into clinical and regulatory deliverables, including Investigator’s Brochures, study protocols, reports, and clinical submission documents, as needed.

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:

• Excellent knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company
• High-level clinical and scientific knowledge of relevant therapeutic areas
• Potential travel to International HQ, congresses and in-country meetings
• Understanding of clinical trial design, regulatory processes, and project management
• A proven track record in team leadership
• Direct involvement with full lifecycle development and medical support of successfully marketed biotechnology or pharmaceutical products
• Genuine concern for patient’s wellbeing and public health
• Time zone flexibility

I would like to submit my application for the medical affairs opening. Please accept this letter and the attached resume.

Previously, I was responsible for regulatory and strategic input on: development concepts and documents and clinical study protocols and protocol amendments.

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

• Proficient public speaking and group discussion facilitation
• Documented successful record track in US Medical Affairs
• Experience with Product Launch is desirable
• Medical, Dental or related scientific filed
• Externally facing role, Technical Expertise
• Proficient in MS-office applications, such as Word, Excel, PowerPoint, etc
• Good at spoken and written English is essential
• Experience with eye care product preferred