Staff Clinician

5 days ago

Rockville, United States PriceSenz Full time
Job DescriptionJob Description

Location : IC: NCI Street: 9609 Medical Center Dr. Bldg.: 9609 Medical Center Dr. Room: TBD City: Rockville State & Zip: MD 20850

Weekly Hours - FT: 30-40 hours per week Total No. of Hours : 40

Overall Position Summary and Objectives

Under this task order the contractor will independently provide support services to satisfy the overall operational objectives of the National Cancer Institute, Division of Cancer Epidemiology and Genetics. The primary objective is to provide services and deliverables through performance of support services.

Min Education - Medical Program

Resume Max Pages - 3

Certifications & Licenses

  • MD

Skills (Ranked by Priority)

  1. Developing and execute strategic and scientific program planning
  2. Conducting program analysis and evaluation
  3. Coordinating multidisciplinary studies
  4. Managing contracts and writing new contracts
  5. Assisting with personnel management

1, 2, 3, 4, 5 represents priority rankings, where 1 is highest priority and 5 is lowest priority of those ranked

Software

  • MS Office

Field of Study

  • Miscellaneous Health Medical Professions

Statement of Work Details

Coordinates all aspects of clinical protocol development, review and implementation.

  • Reviews, assesses, and evaluates clinical and research study design and feasibility. 1
  • Assists the PI in the conceptualization, design, and implementation of multi-disciplinary clinical and research studies with intramural and extramural investigators.
  • Coordinates and manages multi-disciplinary clinical and research studies with intramural and extramural investigators.

Monitors ongoing clinical studies and clinical trials.

  • Identify process and implementation issues/gaps needing attention/remediation; manage their effective escalation and participates in the resolution.

Evaluates existing protocols and provides suggestions for design, execution and improvement.

  • Plan, implement, coordinate and evaluate programs and initiatives in the assigned specialty area of research.
  • Establish goals and objectives for the assigned research area and organize efforts to initiate pioneering programs and resolve critical issues involving accomplishment of the research.
  • Work with staff on protocol development; provide input on study safety design; identify medical and logistical problems that may impede the study; conduct reviews of clinical protocols and all supporting documents; and provide feedback to staff and clinical investigators.

Assists in developing protocols for future clinical projects.

  • Formulate concepts to foster research in new of underdeveloped areas of research.

Produces various detailed reports for use by upper clinic or laboratory management.

  • Review pertinent literature to provide a scientifically rigorous review of the subject matter.

Evaluates various reports and safety monitoring plans and produces detailed reports for use by upper clinic or laboratory management.

  • Analyze data from clinical trials and research investigations; prepare abstracts for submission and manuscripts for publication.

Participates in site visits as needed.

  • Assesses and supports meetings, clinical trial assessments and site visits. 4
  • Attend and participate in specific meetings related to clinical and research studies and assist with gathering information and report status of these studies.

Reviews the clinical protocols for safety of the study.

  • Reviews, evaluates, and analyzes clinical and research data and study information. 2
  • Prepare comprehensive reports and publications related to research and program activities.

Provides advice and guidance for all clinical trials.

  • Advise program management on merits and deficiencies of proposed clinical studies.

Reviews safety reports and provides recommendations for improvement.

  • Provide medical expertise in protocol follow-up stages for subject safety and protection.

Provides guidance to staff on various clinical processes and operational issues.

  • Reviews, evaluates, and recommends logistical, procedural and operational approaches to clinical and research study implementation. 3
  • Advance and ensure a robust and productive research program in collaboration with the PI and other CGB Principal Investigators.

Develops policies and guidelines.

  • Formulates guiding principles and Standard Operating Procedures (SOPs), and prepares staff for clinical research. 5
  • Assist with managing the current clinical support services contract, define problems, analyze alternatives, and recommend solutions to complex issues.

Coordinates and participates in various meetings, training and safety-related educational programs.

  • Attend and participate in scientific meetings and conferences.
  • Collaborate on the planning, development, implementation and administration of research and training programs, projects, and contracts, conferences and workshops.

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