Director Of Clinical Research Resume Example & Writing Guide

Use this Director Of Clinical Research resume example and guide to improve your career and write a powerful resume that will separate you from the competition.

Directors of clinical research oversee the planning, implementation, and evaluation of clinical studies. They’re in charge of managing a team of researchers and ensuring that all study protocols are followed.

Because they play such an integral role in bringing new drugs and medical devices to market, directors of clinical research have the opportunity to have a huge impact on the lives of patients everywhere.

If you’re ready to take on a new challenge and work with some of the brightest minds in the industry, here are some tips for writing a directors of clinical research resume that will help you land the job.

Jennifer Thomas
New York City, NY | (123) 456-7891 | [email protected]

Seasoned director of clinical research with over fifteen years of experience in the pharmaceutical and biotech industries. Proven track record in designing, conducting, and managing clinical trials across a variety of therapeutic areas and indications. Skilled in building and managing cross-functional teams.

Fordham University Jun '07
M.A. in Clinical Psychology
Fordham University Jun '04
B.A. in Psychology
Company A, Director Of Clinical Research Jan '17 – Current
  • Led the clinical research team to develop and implement a new clinical trial for an investigational drug in patients with relapsed/refractory multiple myeloma, resulting in FDA approval of this drug as a treatment option for these patients.
  • Developed and implemented novel methods to improve patient recruitment into clinical trials including partnering with community oncologists to increase awareness about available therapies and increasing the number of sites participating in our studies by over 50%.
  • Collaborated closely with regulatory agencies such as the FDA, EMA, Health Canada, etc., to ensure that all study activities are conducted according to regulations and guidelines.
  • Managed budgets ranging from $1M-$5M per year depending on the phase of development (e.g., Phase I-IV).
  • Oversaw day-to-day operations of Clinical Research department including training staff members, maintaining equipment, ensuring compliance with GCPs/ICH guidelines, etc..
Company B, Director Of Clinical Research Jan '12 – Dec '16
  • Developed and implemented a strategic plan to ensure the timely completion of all clinical research projects
  • Conducted weekly project team meetings to review progress, identify issues and make changes as needed
  • Managed budgets for each project in accordance with company policies and procedures
  • Collaborated with international partners on multi-center studies (France, Germany, UK)
  • Supervised 10+ clinical research associates and junior staff members
Company C, Research Assistant Jan '09 – Dec '11
  • Conducted extensive literature reviews to synthesize data and information on assigned topics.
  • Collected, organized, and analyzed data using various statistical software programs.
  • Prepared research reports, presentations, and summaries of findings for internal and external audiences.
  • Certified Clinical Research Professional (CCRP)
  • Certified Clinical Research Coordinator (CRC)
  • Clinical Research Associate (CRA)

Industry Knowledge: Clinical Trials, Regulatory, Medical Writing, Trial Management, Clinical Documentation
Technical Skills: Microsoft Office Suite, Veeva, Salesforce, Google Analytics, SAS, SPSS, Excel, PowerPoint
Soft Skills: Leadership, Teamwork, Critical Thinking, Problem Solving, Decision Making, Public Speaking, Communication

How to Write a Director Of Clinical Research Resume

Here’s how to write a resume of your own.

Write Compelling Bullet Points

When it comes to bullet points, the more specific you can be, the better. Rather than saying you “managed clinical trials,” you could say that you “managed Phase II clinical trial for new cancer drug, resulting in 100% patient enrollment in six months.”

The second bullet point is much stronger because it provides specific details about what you did and the results of your work. It also includes a quantifiable result (100% patient enrollment).

Identify and Include Relevant Keywords

When you submit your resume for a director of clinical research role, it’s likely that it will be scanned by an applicant tracking system (ATS) for certain keywords. This system looks for certain terms related to the job, like “clinical trials” and “research” in order to determine whether your skills and experience are a match for the position. If you don’t have enough relevant keywords on your resume, the ATS might automatically reject your application.

To increase your chances of getting an interview, make sure to include keywords throughout all sections of your resume. Here are some examples:

  • Clinical Trials
  • Good Clinical Practice (GCP)
  • Clinical Research
  • Clinical Development
  • Clinical Monitoring
  • CRO Management
  • Protocol
  • Data Management
  • Clinical Operations
  • Regulatory Submissions
  • Oncology
  • U.S. Food and Drug Administration (FDA)
  • Biotechnology
  • Pharmacovigilance
  • Medicine
  • Medicine Residency
  • Clinical Data Analysis
  • Regulatory Affairs
  • Electronic Data Capture (EDC)
  • Oncology Clinical Research
  • Clinical Pharmacology
  • Hospitals
  • Medical Writing
  • Clinical Trials Management System (CTMS)
  • Validation
  • Patient Safety
  • Phase I
  • Auditing
  • Medical Education
  • Institutional Review Board (IRB)

Showcase Your Technical Skills

The technical skills section of your resume is one of the most important sections to focus on. As a director of clinical research, you are responsible for the management and implementation of clinical trials. This requires a high level of proficiency in project management software, like Microsoft Project, as well as a solid understanding of statistical analysis software, like SAS and SPSS. Additionally, you should list any other relevant technical skills, like experience with electronic data capture (EDC) systems or clinical trial management systems (CTMS).


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