Nurse Clinical Research I Jobs in Florida

Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.

Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.

Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.

Coordinates with Investigational Pharmacy for subjects to receive required drugs.

Coordinates and submits IRB protocols, reports, revisions, updates, approvals.

Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.

Seeks knowledge and competence that reflects current nursing practice and promotes futuristic thinking.

Collects data pertinent to the healthcare consumer's health or the situation.

Analyzes the assessment data to determine actual or potential diagnoses, problems, and issues.

Identifies expected outcomes for a plan individualized to the healthcare consumer or the situation.

Develops a plan that prescribes strategies to attain expected, measurable outcomes.

Implements the identified plan, coordinates care delivery, and employs strategies to promote health and a safe environment.

Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.

Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.

Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.

Coordinates with Investigational Pharmacy for subjects to receive required drugs.

Coordinates and submits IRB protocols, reports, revisions, updates, approvals.

Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.

$60,000 to $75,000 annually depending on education and experience.

Provides coverage for Research Manager and the Principal Investigator.

Bachelor's Degree in nursing and two years of professional nursing experience.

Two years prior experience with clinical trials, experience with HIV/AIDS clinical trials is preferred but not requires.

Updates study schemas/source documentation for studies and assists with overall QA activities for the program.

Maintains monthly billing for study visits and documents appropriate fees on research referral forms.

Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.

Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.

Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.

Coordinates with Investigational Pharmacy for subjects to receive required drugs.

Coordinates and submits IRB protocols, reports, revisions, updates, approvals.

Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.

Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.

Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.

Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.

Coordinates with Investigational Pharmacy for subjects to receive required drugs.

Coordinates and submits IRB protocols, reports, revisions, updates, approvals.

Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.