Over 1 Million Paying Vacancies Available. Discover Your Dream Vacancy with Us!

Are you looking for a Clinical Trials Specialist? We suggest you consider a direct vacancy at National Institutes of Health in Montgomery County. The page displays the terms, salary level, and employer contacts National Institutes of Health person

Job opening: Clinical Trials Specialist

Salary: $99 200 - 153 354 per year
Published at: Jul 08 2024
Employment Type: Full-time
This position is located in the Center for the Clinical Trials Network (CCTN), National Institute on Drug Abuse (NIDA). The CTN is a community-based research infrastructure to 1) conduct clinical studies of promising therapies for drug addiction and 2) ensure the timely transfer of research results to physicians, providers, and their patients.

Requirements

  • U.S. Citizenship requirement or proof of being a U.S. National must be met by closing date.
  • Employment is subject to the successful completion of a background investigation, verification of qualifications, completion of onboarding forms, submission of required documents, and any other job-related requirement before or after appointment.
  • Applicants must meet all qualification requirements by the closing date of this announcement.
  • Males born after December 31, 1959 must be registered with the Selective Service.
  • Position requires Education.

Qualifications

Basic Education Requirement: In order to qualify for a Clinical Trials Specialist GS-601 position, you must have successfully completed a bachelor's degree or graduate/higher level degree with major study in an academic field related to the medical field, health sciences or allied sciences appropriate to the work of the position. (This degree must be from an educational program from an accrediting body recognized by the U.S. Department of Education at the time the degree was obtained). Additional Qualifications: You qualify at the GS-12 level, if you meet the following: You must demonstrate in your resume at least one (1) year of specialized experience equivalent to at least the GS-11 level in the Federal service obtained in either the private or public sector, performing the following types of tasks: preparing comprehensive reports summarizing the progress on clinical trials; conducting clinical trials and targeted research programs; assisting in protocol development, implementation, clinical site monitoring, and contributing to the presentations of clinical research. You qualify at the GS-13 level, if you meet the following: You must demonstrate in your resume at least one (1) year of specialized experience equivalent to at least the GS-12 level in the Federal service obtained in either the private or public sector, performing the following types of tasks: preparing Investigational New Drug (IND) applications and Clinical Trial Agreements; performing oversight and management pertaining to the regulatory and procedural aspects of clinical research/clinical trials; developing protocol budgets; managing protocol development for clinical studies and monitoring performance; and establishing overall priorities for the oversight of clinical trials and performance evaluation. You will receive credit for all experience material to the position, including experience gained in religious, civic, welfare, service, and organizational activities, regardless of whether you received pay. Do not copy and paste the duties, specialized experience, or occupational assessment questionnaire from this announcement into your resume as that will not be considered a demonstration of your qualifications for this position. To determine your qualifications and referral status, we may review your resume and supporting documentation and compare it against your responses to the vacancy questionnaire. Ensure you support your self-ratings with the information you provide in your application. We may verify or assess your qualifications at any time. Inflated or unsupported qualifications may affect your rating. Any misrepresentation or material omission of facts may be sufficient cause to end further consideration of your candidacy. Persons listed as knowing your past accomplishments or experience in your application may be contacted for verification purposes at any time. Verification may, but need not, begin before receiving an offer. Preview assessment questionnaire before you apply: https://apply.usastaffing.gov/ViewQuestionnaire/12402106

Education

This position has an education requirement. You are strongly encouraged to submit a copy of your transcripts (or a list of your courses including titles, credit hours completed and grades). Unofficial transcripts will be accepted in the application package. Official transcripts will be required from all selectees prior to receiving an official offer. Click here for information on Foreign Education.

Contacts

  • Address National Institutes of Health 6701 Rockledge Drive Bethesda, MD 20892 US
  • Name: Jessica Phillips
  • Email: [email protected]

Map

Similar vacancies

Director, Office of Science Policy, Planning, Evaluation and Reporting (OSSPER), NIMHD Sep 05 2024
$169 964 - 191 900

Leads and manages the scientific reporting, strategic planning, science policy, and evaluation in support of the mission of NIMHD. Coordinates the strategic...

Supervisory Radiological Specialist Mar 14 2024
$163 964 - 191 900

Performing programmatic and management duties for the Department and supervises the department’s functions and staff through subordinate supervisors. ...

Deputy Director Mar 11 2024
$163 964 - 191 900

Serve as a critical advisor for the Director of the Office of Clinical Research on clinical research issues with a particular focus on the design of clinical trials, the protection of participants i...

Supervisory Clinical Informaticist Feb 15 2024
$163 964 - 191 900

The Chief of Clinical Informatics participates with the CIO in policy development and guidance, program direction, and the exercise of departmental authority over the clinical information systems th...

Supervisory Health Science Policy Analyst Mar 11 2024
$163 964 - 191 900

Serve as a critical advisor for the Director of the Office of Clinical Research on clinical research issues with a particular focus on the design of clinical trials, the protection of participants i...