Research Coordinator Nurse Bookmark this Posting Print Preview | Apply for this Job

Posting Details

Position Information

About MSM

Morehouse School of Medicine ( MSM ) is a place of distinction, serving as the nation’s leading academic medical center for vulnerable populations. It’s also a place for passionate individuals looking to join a dedicated community working today to help prepare tomorrow’s leaders.

We exist to:

• Improve the health and well-being of individuals and communities;

• Increase the diversity of the health professional and scientific workforce;

• Address primary health care through programs in education, research and service;

With emphasis on people of color and the under-served urban and rural populations in Georgia, the nation and the world.

At Morehouse School of Medicine, we’re leading the creation and advancement of health equity. You will find a fulfilling career at MSM !

Posting Number NONAC3229

Job Title Research Coordinator Nurse

Position Title Research Coordinator Nurse

Position Type Non-Faculty

Number of vacancies 1

Salary Commensurate with experience

Department Clinical Rsch Ctr-CRC

Position Summary

The Research Nurse Coordinator works under the direction of the Principal Investigator and plays an integral role in the management of research studies. As an essential part of the research team she utilizes highly acquired skills to aid in research development, and to successfully achieve research program goals.

Minimum Qualifications

Experience:

• License Practical Nurse or Registered Nurse with current license to practice in the state of Georgia

• 5 years of experience nursing experience

  Preferred Qualifications

  Closing Date

  Open Until Filled No

  Special Instructions to Applicants

  Quick Link https://careers.msm.edu/postings/19822

  EEO Statement Summary

Morehouse School of Medicine is an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all Federal and Georgia State laws, regulations, and executive orders regarding non-discrimination and affirmative action. Morehouse School of Medicine does not discriminate on the basis of race, age, color, religion, national origin or ancestry, sex, gender, disability, veteran status, genetic information, sexual orientation, or gender identity or expression.

Job Duties

Description of Job Duty

• Coordinates with Principal Investigator to ensure that clinical research and related activities are performed in accordance with federal regulations and sponsoring agency policies and procedures.

• Assists the PI in development of materials that meet protocol requirements, schedule of visits, and execution of research plan.

• Provides appropriate training and tools for study team members.

• Documents date of training and signatures of study personnel trained on study specific training log.

• Ensures compliance and monitors efforts related to human research participant protection and reports instances of noncompliance to the appropriate compliance office.

• Reviews and comprehends the protocol.

• Attends investigator meetings as required or requested by the PI.

• Prepare IRB and any other regulatory submission documents per the protocol.

• Prepares study materials such as the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs, establishes and organizes study files, regulatory binders, study specific source documentation and other materials.

• Coordinates with Principal Investigator institution, department, and central administration to help ensure that clinical research and related activities are performed in accordance with federal regulations, university and sponsoring agency policies and recruitment strategies in accordance with IRB requirements and approvals.

• Screens subjects for eligibility using protocol specific inclusion and exclusion criteria.

• Coordinates participant tests and procedures.

• Perform Nursing duties as required by study protocol, including but not limited to, administering of Investigational Product, application of Investigational Device, venipuncture for the collection of blood samples, other types of sample collection and laboratory processing, packaging and shipment of samples.

• Collects data as required by the protocol.

• Assures timely completion of Case Report Forms.

• Maintains effective and ongoing communication with sponsor, research participants and PI during the study.

• Is responsible for maintaining adequate inventory of study supplies, coordinates the management of investigational drugs/devices according to sponsor protocol.

• Organizes Monitor’s site visits, make correction to deficiencies.

• At the end of the study completes study documentation and maintains study files in accordance with sponsor requirements.

• Retains all study records in accordance with sponsor requirements and the Clinical Research Center’s policies and procedures.

• Performs all tasks as assigned by management.

  Pre-Employment/Employment Requirements

All offers of employment are contingent upon successful completion of all pre-employment screenings.

Immunization

Immunization Requirements

It is MSM’s Immunization policy that all Prospective Employees are required to provide proof that they are vaccinated against COVID -19 prior to commencement of employment. If employment will commence during Flu Season, MSM requires all individuals to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless granted an exemption. Failure to provide proof of vaccination for any required vaccines or obtain an exemption from MSM will result in rescission of a candidate’s offer of employment or disciplinary action up to and including termination.

Posting Specific Questions

Required fields are indicated with an asterisk (*).

• • What is your salary expectation?

(Open Ended Question) Applicant Documents Required Documents

• Curriculum Vitae or Resume

  Optional Documents

• Cover Letter