Clinical Trial Research Nurse I Jobs

Bachelor’s Degree in Nursing preferred. Equivalent education, experience and/or training may be substituted for the degree requirement.

Two or more years of nursing experience working in a hospital setting.

Minimum of 1 year or more years of experience working in an Oncology specialty area in a hospital or clinic setting.

Minimum of 6 months of clinical research nursing experience.

Maintains active Basic Life Support (BLS) certification.

Must possess excellent communication and interpersonal skills to interact with subjects in a clear and confident manner.

Provides medication management services to clients with mental or emotional disorders

Provides case management services to selected clientele

Provides patient counseling and education related to clinical care needs

No first-time homebuyer requirement to qualify.

Orders and stocks clinic supplies and medications

Administers psychotropic medications and monitors side effects

7. Assists investigator with correspondence with IRB. (essential)

4. Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.

3. Potential exposure to adverse environmental conditions

o Several times a month: Radiation-irradiator possible.

Use problem solving skills to help patients overcome obstacles to enrollment

Maintain/increase knowledge and understanding of hematologic cancers, blood and bone marrow transplant and psychosocial aspects of living with cancer

Outstanding critical thinking, problem-solving, and collaboration skills

Demonstrated commitment to independent learning and skill enhancement

Serve in consulting role to the Information Resource Center about clinical trials

Contribute to continual process improvement of clinical trial support procedures

Preferred Education, Experience and Skills:

Excellent clinical, analytical and organizational skills with demonstrated research nursing ability. Working knowledge of clinical trials administration.

Proven ability to manage several projects concurrently while balancing competing priorities and deadlines.

Comprehensive Cancer Center – Clinical Trial Operations

None - Not included in the union (Yale Union Group)

YCC Clinical Research Nurse (P5)

This position will coordinate care of patients of other research coordinators within the Division as needed.

This position will perform other duties as assigned by the Supervisor, Clinical Trials Unit.

"In order to be considered, you must upload your resume."

Application must be submitted by 11:55 p.m. (ET) of the posting end date.

2+ years of peds experience

Recent experience in drawing blood

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Collecting samples and required information and data

IP preparation, administration, and post observation (1 hour)

Labelling and shipment of samples

Excellent clinical, analytical and organizational skills with demonstrated research nursing ability. Working knowledge of clinical trials administration.

Proven ability to manage several projects concurrently while balancing competing priorities and deadlines.

Comprehensive Cancer Center - Clinical Trial Operations

None - Not included in the union (Yale Union Group)

YCC Clinical Research Nurse (P5)

Click here to see our Wage Ranges

Must meet all unit specific certification requirements: (PALS, ACLS, NRP)

Must complete all of the Nurse Residency Program Requirements

Ability to learn and use computer systems in order to manage patient information

Demonstrated effective interpersonal, verbal and written communications skills

Reports to Nurse Manager/Charge Nurse of unit to which assigned.

An Associate Degree in Nursing is required; Bachelor of Science from a College of Nursing is preferred.

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.

With supervision, assist in the accurate and appropriate study test article management.

Support the effective financial management of the clinical trial.

Other duties as assigned by appropriate management.

Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.

With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.

No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.

What are the top 5 skills/requirements this person is required have?

What level of education, type of degree and/or certification is required? Nursing, RN.

Required Skill 1: Communication skills

Required Skill 2: Listening and answering volunteer questions

Required Skill 3: Customer Service skills

Required Skill 5: Nursing skills

Assist with training of other staff (e.g., doulas) in cardiovascular health coaching protocols and blood pressure self-management.

Provide in-person and telephonic health coaching and education around diet, physical activity and weight control goals

Possesses excellent communication and interpersonal skills.

Experience with culturally responsive interventions

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Connect participants with community resources/referrals as needed, including transportation, personal care needs, social services, etc

Answers queries in accordance with protocol requirements.

Basic Life Support (BLS) Certification.

One year of relevant experience.

Documents clinical research data in electronic data capture (EDC) and/or iMedidata Rave.

Provides outreach in the community to enhance enrollment.

Regularly provides updates, follows-up on projects and ensures deadlines are met by all stakeholders as required.

Strong organizational and time management skills

Ensure strict compliance with established research protocols and standards along with all applicable laws, regulations, policies, and procedural requirements

Follow established SOPs, GCP and other applicable regulatory requirements in the execution of all research activities.

Minimum 2 years of nursing experience

Excellent written and verbal communication skills

Knowledge of clinical research operations, including Good Clinical Practice guidelines is preferred

Bilingual skills to communicate effectively with patients and families Understanding of JCAHO requirements

1 year of outpatient and inpatient clinical nursing experience in adult acute care

• Clinical Research Certification • Basic Life Support • Advanced Cardiac Life Support

Background Check and Live Scan

Legal Right to work in the United States

California Child Abuse and Neglect Reporting Act

Completes nursing history and initiates patient education.

Collaborates with interdisciplinary team members.

Implements plan of care appropriate to diagnosis. Evaluates care outcomes.

Problem solves and coordinates unit/patient care assignments, with supervision.

Introduces new employees/students to unit routines.

Supervises LPNs, Nursing Assistants, HUCs, Techs and sitters.