Clinical Advisor

4 weeks ago

Bethesda, United States Rays TechServ Pvt. Ltd. Full time

Technical Requirements: Clinical Advisor
- Implement and coordinate a range of individual clinical site-management activities.
- Advise PIs on clinical site start-up and relevant operational and regulatory issues including resource allocation, and administrative issues.
- Provide leadership for planning, organizing, and conducting site visits or reverse site visits as appropriate to clinical trials units/clinical research sites to effectively fulfill site management responsibilities.
- Assess the level of clinical trials research competency of clinical research site staff and the extent of research knowledge and technology available to achieve the desired quantity and quality of research to be conducted at the clinical research sites.
- Evaluate clinical trials units/clinical research sites’ organizational structures and modes of operations in relationship to the achievement of the Division’s goals and objectives in the areas of administration, clinical site management, and recruitment of patients.
- Provide oversight and technical direction for evaluation of site performance.
- Identify problems or issues that transcend individual units or trends that indicate the need for procedural clarification or policy development and recommends follow-up actions or policy directives to OCSO Director or Branch Chief.
- Conduct trainings at sites and Network meetings on relevant policies/regulations.
- Attend local Network meetings, conference calls, ad hoc meetings and working groups.
- Support federal Program Officers by: 1) tracking and summarizing grantee compliance with training requirements, grantee progress in meeting the grant aims by reviewing progress reports, and adherence to applicable regulations; and 2) reviewing and providing input on training materials, policies and procedures.
- Participate in the creation and review of site development and site closure-related documents and checklists.
- Interface with networks, investigators, Operations Centers, to share information and collaborate on research and site-related issues.
- Prepare oral and written presentations for internal and external programmatic and scientific meetings.

Specific Qualifications:

- Minimum of a BS degree in a science or health related discipline.
- Minimum of five (5) years of progressive experience in managing clinical trials/clinical research sites and/or monitoring clinical trials.

**Salary**: $70,000.00 - $90,000.00 per hour

**Benefits**:

- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance

Medical specialties:

- Home Health

Physical setting:

- Clinic

Standard shift:

- Day shift

Weekly schedule:

- Monday to Friday

**Experience**:

- clinical trials: 5 years (required)
- clinical research: 5 years (required)
- Clinical Site Management: 5 years (required)

License/Certification:

- BLS Certification (preferred)
- RN (preferred)

Ability to Commute:

- Bethesda, MD 20817 (required)

Ability to Relocate:

- Bethesda, MD 20817: Relocate before starting work (required)

Work Location: In person

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