Clinical Researcher Resume Sample

4.8
18 votes
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Abe Yost
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Work Experience


Senior Clinical Quality Researcher
09/2015 - PRESENT
San Francisco, CA
  • Contribute to RTI’s scientific stature by presenting papers and posters at conferences, and engaging in internal presentations/seminars
  • Demonstrated experience in developing clinical quality measures and/or clinical quality improvement efforts guided by quality, safety, or other performance metrics
  • Experience assessing clinical workflows related to measurement concepts or performance metrics
  • Extensive experience in client-facing situations and successful history of communicating findings to clients and decision makers
  • Experience planning, motivating, and supervising the work of large teams
  • Experience with the NQF endorsement process and/or CMS Measures Management System Blueprint
  • Experience and knowledge of CMS, state, and other quality reporting programs. Working knowledge of standards used in quality measure development
Clinical Researcher
11/2010 - 04/2015
New York, NY
  • Strong organizational skills and high level of attention to detail; flexibility to lead and manage multiple priorities, sometimes simultaneously, under deadlines
  • Develop study protocol
  • Co-develop the Statistical Analysis Plan
  • Interpretation of the study results
  • Writing of study report
  • Build internal and external network of investigators/experts and other stakeholders
  • Data interpretation and to translate this to the manuscript
Clinical Intelligence Researcher
04/2004 - 05/2010
Philadelphia, PA
  • Communication of study results
  • Support clinical study protocol writing
  • Support clinical report writing
  • Assist in study/protocol development and preparation, including developing of new research SOPs when required, review/modification of research protocols, writing of informed consent documents, and design of case report forms (CRFs)
  • Perform and/or study coordination, including scheduling of protocol-specific screening and follow-up visits and performing interval interviews and assessments at study visits for protocol-specific data
  • Maintain Complete Study Documentation, including subjects’ reports and progress notes, and document protocol deviations
  • Monitor Test Article Accountability, including storage and accountability log if the study includes a test article
  • Ensure proper collection, processing and shipment of laboratory specimens collected during the study
  • Assist in Recording and Reporting of Study Adverse Events

Education


Shawnee State University
2000 - 2004
Bachelor's Degree in Nursing

Professional Skills


  • Demonstrated ability to organize office and develop procedures; maintain and/or develop complex paper and electronic record management filing systems
  • Experience in (international) clinical research
  • Experience in infectious disease, oncology, behavioral health and/or HIV
  • Live near or willing to relocate to the greater Kansas City, MO area
  • Create or modify Informed Consent documents that comply with HRPP, FDA and other governing agencies
  • Thorough knowledge of methodology and statistics
  • Engagement in research projects with the CDC, NIH and/or similar organizations

How to write Clinical Researcher Resume

Clinical Researcher role is responsible for training, research, clinical, events, travel, modeling, design, reporting, shipping, health.
To write great resume for clinical researcher job, your resume must include:

  • Your contact information
  • Work experience
  • Education
  • Skill listing

Contact Information For Clinical Researcher Resume

The section contact information is important in your clinical researcher resume. The recruiter has to be able to contact you ASAP if they like to offer you the job. This is why you need to provide your:

  • First and last name
  • Email
  • Telephone number

Work Experience in Your Clinical Researcher Resume

The section work experience is an essential part of your clinical researcher resume. It’s the one thing the recruiter really cares about and pays the most attention to.
This section, however, is not just a list of your previous clinical researcher responsibilities. It's meant to present you as a wholesome candidate by showcasing your relevant accomplishments and should be tailored specifically to the particular clinical researcher position you're applying to. The work experience section should be the detailed summary of your latest 3 or 4 positions.

Representative Clinical Researcher resume experience can include:

  • Experience in statistics or quantitative research
  • Coordinate Study Close-Out, including sponsor/monitor closeout visit
  • Prepare Monthly Activity Reports, Screening and Volunteer Disposition logs, and Help Compile Final and Annual Reports for the Study
  • Serve as projects principle point of contact for regulatory affairs, quality assurance and clinical monitoring issues, reviews, audits, reports, etc
  • Coordinates and/or participates in the conduct of clinical research studies as a Project team member and, as directed, a team leader
  • Coordinates/ performs and/or provides regulatory oversight of study activities in accordance with the approved protocols

Education on a Clinical Researcher Resume

Make sure to make education a priority on your clinical researcher resume. If you’ve been working for a few years and have a few solid positions to show, put your education after your clinical researcher experience. For example, if you have a Ph.D in Neuroscience and a Master's in the same sphere, just list your Ph.D. Besides the doctorate, Master’s degrees go next, followed by Bachelor’s and finally, Associate’s degree.

Additional details to include:

  • School you graduated from
  • Major/ minor
  • Year of graduation
  • Location of school

These are the four additional pieces of information you should mention when listing your education on your resume.

Professional Skills in Clinical Researcher Resume

When listing skills on your clinical researcher resume, remember always to be honest about your level of ability. Include the Skills section after experience.

Present the most important skills in your resume, there's a list of typical clinical researcher skills:

  • Demonstrated experience creating or modifying Informed Consent documents that comply with HRPP, FDA and other governing agencies
  • (Medical) writing skills
  • Experience managing projects and client/cooperative relationships
  • Experience in statistics or quantitative research
  • Experience in statistics, quantitative or clinical research
  • Demonstrated ability to set short and long-term goals of projects and project objectives, and work with others in achieving organizational goals and deadlines

List of Typical Experience For a Clinical Researcher Resume

1

Experience For Clinical Quality Researcher Resume

  • Shall participate in the development of study plans and necessary infrastructure for the implementation of approved clinical studies/protocols
  • Perform as liaison between study sites as required
  • Provide training sessions to extramural sites on GCP and protocol related training including human subjects’ protection/ethics training and study specific training
  • Provide administrative and logistics support for conduct of meetings and conferences

List of Typical Skills For a Clinical Researcher Resume

1

Skills For Clinical Quality Researcher Resume

  • Understanding of SOP for conducting human subjects research
  • International Air Transportation Association (IATA) certification to oversee shipping of biological substances
  • Basic competency in SAS
  • Master’s in Statistics, Epidemiology, Public Health, MSN or related relevant field
  • Travel up to 25 %
  • Experience with multiple clinical research projects with complex logistics involving multi-sites and priorities. Ability to work with others in achieving organizational goals and deadlines
  • Knowledge of neurological disease such as Parkinson's, dementia, Atypical Parkinson's Disorders, Progressive Supranuclear Palsy, Corticobasal Degeneration, Multiple System Atrophy, Alzheimer’s Disease, Lewy Body Disease and other related disorders
2

Skills For Clinical Intelligence Researcher Resume

  • Excellent interpersonal skills including tact, diplomacy and flexibility. Ability to work independently and/or in a team framework in conjunction with principles of community and in a clinical research environment that interacts with a diverse group of researchers, technical personnel and others. Ability to maintain confidentiality as required
  • Knowledge of neurological disease such as Parkinson’s disease, dementia, atypical parkinsonian disorders, progressive supranuclear palsy, corticobasal degeneration, multiple system atrophy, Alzheimer’s disease, Lewy body disease and other related disorders
  • Experience and familiarity with the Institutional Review Board. Experience preparing and submitting continuing review materials, amendments, and other regulatory documents to an IRB
  • Proven ability to read, understand, and learn study procedures from protocols. Strong problem-solving and decision-making skills. Ability to create or modify Informed Consent documents that comply with HRPP, FDA and other governing agencies
  • Strong expertise with personal computers and software programs (including Word, Excel, Powerpoint). Ability to organize office and develop procedures; maintain and/or develop complex paper and electronic record management filing systems
  • Research, gather, evaluate, and organize information to produce clear and concise protocol reports using various resources and to perform tasks accurately and quickly, disseminate information effectively whether in report form or via presentation
  • Strong ability to write policies, business correspondence, reports and procedure manuals, experience with editing and/or proofreading documents, fast and accurate typing skills; excellent grammatical and proofreading skills
3

Skills For Senior Clinical Quality Researcher Resume

  • Excellent interpersonal, oral and written communication skills, including diplomacy, tact, and flexibility. Ability to interact with all organizational levels and to communicate effectively and professionally both in person and via phone
  • Strong phone etiquette. Ability to present a positive impression in person, on the telephone, and through email. Experience working in a team-oriented environment as well as work independently
  • Project management experience with ability to successfully plan, organize, prioritize, develop, analyze, implement and manage multiple clinical research projects with complex logistics involving multi-sites and priorities
  • Strong experience working with clinical trials research activities, regulatory compliance, guidelines related to informed consent, ethical conduct, and protection of human subjects as well as interpreting and comprehending complex clinical research protocols, activities and guidelines
  • Demonstrated working knowledge of Good Clinical Practice. Proven ability to abstract information from protocol and investigators brochures to create a stand-alone Research Plan
  • Research information, and to develop responsive, creative, innovative, and effective solutions and analyze data to arrive at valid conclusions, recommendations and plans of actions. Detail oriented, logical and methodological approach to problem solving. Strong process orientation
4

Skills For Clinical Study Researcher Resume

  • Proven experience and familiarity with the Institutional Review Board. Experience preparing and submitting continuing review materials, amendments, and other regulatory documents to an IRB
  • Strong ability to write policies, business correspondence, reports and procedure manuals, experience with editing and/or proofreading documents, fast and accurate typing skills. Excellent grammatical and proofreading skills
  • Excellent oral and written communication skills. Ability to interact with all organizational levels and to communicate effectively and professionally both in person and via phone. Solid phone etiquette. Ability to present a positive impression in person, on the telephone, and through email
  • Proven ability to research, gather, evaluate, and organize information to produce clear and concise protocol reports using various resources and to perform tasks accurately and quickly, disseminate information effectively whether in report form or via presentation
  • Demonstrated expertise with personal computers and software programs, including Word, Excel, Powerpoint and database software
  • Demonstrated ability to organize office, and maintain and/or develop complex paper and electronic record management filing systems
  • Excellent interpersonal skills including tact, diplomacy and flexibility. Ability to work independently and/or in a team framework in conjunction with principles of community and in a clinical research environment that interacts with diverse group of researchers, technical personnel and others. Ability to maintain confidentiality as required
5

Skills For Clinical Researcher Resume

  • Experience with protocol writing
  • Experience in study report writing is a pre
  • Experience with phase I studies
  • PhD with minimal of 2 years additional experience
  • Experience with clinical studies
  • Experience with Alzheimer’s disease or Neurology is a benefit
6

Skills For Clinical Quality Researcher Resume

  • Dedicated to writing reports and manuscripts
  • A Certified Clinical Research Professional (CCRP) certificate
  • Knowledge of study methodology and statistics

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