10 days old

Research Nurse

Dartmouth College
Hanover, NH 03755
  • Job Code
    115862848


Dartmouth College



Dartmouth College is an equal opportunity/affirmative action employer with a strong commitment to diversity. In that spirit, we are particularly interested in receiving applications from a broad spectrum of people, including women, minorities, individuals with disabilities, veterans or any other legally protected group.

Position Information

Position Title
Research Nurse

Department
Epidemiology

Position Number
1127053

Position Purpose

To implement the ongoing activities for a National Institute of Health (NIH) reproductive health study.



SEIU Level
Not an SEIU Position

FLSA
Exempt

Employment Category
Regular Part Time

Department Contact for Cover Letter
Amy DeSantis

Special Instructions to Applicants

This position is funded by a grant. Continuation is based upon available funds.

Employment in this position is contingent upon consent to and successful completion of a pre-employment background check, which may include a criminal background check, reference checks, verification of work history, and verification of any required academic credentials, licenses, and/or certifications, with results acceptable to Dartmouth College. A criminal conviction will not automatically disqualify an applicant from employment. Background check information will be used in a confidential, non-discriminatory manner consistent with state and federal law.



Key Accountabilities

Key Accountabilities

Coordination

  • Implements the research activities with participating medical clinics including distribution and completion of surveys, data collection and management, subject identification and recruitment, interviewing and scheduling.
  • Develops and maintains working relationships with collaborating clinics and hospital staff to ensure accurate screening, recruitment and follow up activities according to study protocols and current clinical best practices.
  • Acts as a resource to collaborating clinics, hospital staff, and other study staff on clinical aspects of the study, study protocols and processes.
  • Provides training as needed with respect to clinical procedures, EMR review and other aspects of study protocols.
  • Works closely with principal investigator on development of, revisions and updates to protocols, study materials and supplies.
  • Maintains close communication with Principal investigator, study research director and other study staff regarding study progress, processes, collection and delivery of samples and needed supplies and materials.
  • Coordinates and conducts chart review scheduling and other activities with hospital personnel.
  • Assists study research director with data monitoring and tracking activities, preparation of reports, Institutional Review Board ( IRB ) renewals and revisions and coordination of other administrative activities as needed.
  • Coordinates collection and delivery of samples with laboratory, clinics, hospital staff and other study staff.
  • Maintains study supplies and materials at participating sites.

Recruitment, Interviewing and Specimen Collection

  • Responsible for recruitment, enrollment and interviewing of study participants.
  • Conducts complex pediatric and maternal assessments.
  • Coordinates recruitment and interview schedule with clinic staff.
  • Maintains high level of participant enrollment through effective recruitment and retention strategies.
  • Provides education and instruction to participants on informed consent, study materials, collection of samples, and follow up processes according to protocols.
  • Obtains participant data and specimens through structured interview and delivery room procedures. Assures participant self-administered surveys and specimen collection activities are completed accurately. Conducts necessary follow up activities as needed and coordinates with laboratory and other study personnel to assure specimens are collected, processed and delivered according to protocol.
  • Processes biologic samples and performs other laboratory procedures required for the study.
  • Enters accurate study data in establish database in a timely manner according to protocols.

Medical Records

  • Conducts prenatal, delivery and postpartum medical record reviews for both mother and infant according to study protocols and acts as a clinical resource to other study staff for medical record reviews.
  • Abstracts clinical history and patient outcome data from medical records according to study protocols and enters in established database.
  • Maintains working relationships with medical and administrative staff to coordinate medical record review activities.

Data Management

  • Assures that data are successfully collected and managed.
  • Assures that subject and data confidentiality is maintained and data integrity is maintained.
  • Generates pertinent reports on a monthly or as needed basis.
  • Assists in the organization of study related protocols on the server.
  • May assist in the supervision of students or other temporary staff performing study related tasks.

Project Support

  • Drafts study documents, including protocols, questionnaires and other materials.
  • Acts as the primary clinical resource to the principal investigator and study team members for all aspects of the study and develops protocols to reflect current clinical practice and procedures.
  • Solicits review of developed materials by study team.
  • Coordinates periodic review and update of protocols and assists in preparation of materials for IRB requests and renewals.
  • Maintains accurate and efficient tracking system for study documents approved by IRB and assures protocol materials are update to date and distributed appropriately.
  • Coordinates mailings for study subjects, follows up with staff on missing forms and materials and maintains supply of materials for staff.

Miscellaneous

  • Conducts literature reviews under the direction of the Principal Investigator and/or Research Director in support of study related topics.
  • May assist with statistical analyses and preparation of manuscripts for publication.
-- Demonstrates a commitment to diversity, inclusion, and cultural awareness through actions, interactions, and communications with others. -- Performs other duties as assigned.

PI115862848

<br/><br/><b>Dartmouth College</b><br/><br/><br/><br/>Dartmouth College is an equal opportunity/affirmative action employer with a strong commitment to diversity. In that spirit, we are particularly interested in receiving applications from a broad spectrum of people, including women, minorities, individuals with disabilities, veterans or any other legally protected group.<br/><br/><b>Position Information</b><br/><br/><b>Position Title</b><br/>Research Nurse<br/><br/><b>Department</b><br/>Epidemiology<br/><br/><b>Position Number</b><br/>1127053<br/><br/><b>Position Purpose</b><br/><p>To implement the ongoing activities for a National Institute of Health (NIH) reproductive health study.</p><br/><br/><b>SEIU Level</b><br/>Not an SEIU Position<br/><br/><b>FLSA</b><br/>Exempt<br/><br/><b>Employment Category</b><br/>Regular Part Time<br/><br/><b>Department Contact for Cover Letter</b><br/>Amy DeSantis<br/><br/><b>Special Instructions to Applicants</b><br/><p>This position is funded by a grant. Continuation is based upon available funds.</p> <p>Employment in this position is contingent upon consent to and successful completion of a pre-employment background check, which may include a criminal background check, reference checks, verification of work history, and verification of any required academic credentials, licenses, and/or certifications, with results acceptable to Dartmouth College. A criminal conviction will not automatically disqualify an applicant from employment. Background check information will be used in a confidential, non-discriminatory manner consistent with state and federal law.</p><br/><br/><b>Key Accountabilities</b><br/><p></p> <tr> <th>Key Accountabilities</th> <td><p>Coordination</p> <ul> <li>Implements the research activities with participating medical clinics including distribution and completion of surveys, data collection and management, subject identification and recruitment, interviewing and scheduling.</li> <li>Develops and maintains working relationships with collaborating clinics and hospital staff to ensure accurate screening, recruitment and follow up activities according to study protocols and current clinical best practices.</li> <li>Acts as a resource to collaborating clinics, hospital staff, and other study staff on clinical aspects of the study, study protocols and processes.</li> <li>Provides training as needed with respect to clinical procedures, EMR review and other aspects of study protocols.</li> <li>Works closely with principal investigator on development of, revisions and updates to protocols, study materials and supplies.</li> <li>Maintains close communication with Principal investigator, study research director and other study staff regarding study progress, processes, collection and delivery of samples and needed supplies and materials.</li> <li>Coordinates and conducts chart review scheduling and other activities with hospital personnel.</li> <li>Assists study research director with data monitoring and tracking activities, preparation of reports, Institutional Review Board ( IRB ) renewals and revisions and coordination of other administrative activities as needed.</li> <li>Coordinates collection and delivery of samples with laboratory, clinics, hospital staff and other study staff.</li> <li>Maintains study supplies and materials at participating sites.</li> </ul> <p>Recruitment, Interviewing and Specimen Collection</p> <ul> <li>Responsible for recruitment, enrollment and interviewing of study participants.</li> <li>Conducts complex pediatric and maternal assessments.</li> <li>Coordinates recruitment and interview schedule with clinic staff.</li> <li>Maintains high level of participant enrollment through effective recruitment and retention strategies.</li> <li>Provides education and instruction to participants on informed consent, study materials, collection of samples, and follow up processes according to protocols.</li> <li>Obtains participant data and specimens through structured interview and delivery room procedures. Assures participant self-administered surveys and specimen collection activities are completed accurately. Conducts necessary follow up activities as needed and coordinates with laboratory and other study personnel to assure specimens are collected, processed and delivered according to protocol.</li> <li>Processes biologic samples and performs other laboratory procedures required for the study.</li> <li>Enters accurate study data in establish database in a timely manner according to protocols.</li> </ul> <p>Medical Records</p> <ul> <li>Conducts prenatal, delivery and postpartum medical record reviews for both mother and infant according to study protocols and acts as a clinical resource to other study staff for medical record reviews.</li> <li>Abstracts clinical history and patient outcome data from medical records according to study protocols and enters in established database.</li> <li>Maintains working relationships with medical and administrative staff to coordinate medical record review activities.</li> </ul> <p>Data Management</p> <ul> <li>Assures that data are successfully collected and managed.</li> <li>Assures that subject and data confidentiality is maintained and data integrity is maintained.</li> <li>Generates pertinent reports on a monthly or as needed basis.</li> <li>Assists in the organization of study related protocols on the server.</li> <li>May assist in the supervision of students or other temporary staff performing study related tasks.</li> </ul> <p>Project Support</p> <ul> <li>Drafts study documents, including protocols, questionnaires and other materials.</li> <li>Acts as the primary clinical resource to the principal investigator and study team members for all aspects of the study and develops protocols to reflect current clinical practice and procedures.</li> <li>Solicits review of developed materials by study team.</li> <li>Coordinates periodic review and update of protocols and assists in preparation of materials for IRB requests and renewals.</li> <li>Maintains accurate and efficient tracking system for study documents approved by IRB and assures protocol materials are update to date and distributed appropriately.</li> <li>Coordinates mailings for study subjects, follows up with staff on missing forms and materials and maintains supply of materials for staff.</li> </ul> <p>Miscellaneous</p> <ul> <li>Conducts literature reviews under the direction of the Principal Investigator and/or Research Director in support of study related topics.</li> <li>May assist with statistical analyses and preparation of manuscripts for publication.</li> </ul></td> </tr> <tr> <th>--</th> <td>Demonstrates a commitment to diversity, inclusion, and cultural awareness through actions, interactions, and communications with others.</td> </tr> <tr> <th>--</th> <td>Performs other duties as assigned.</td> </tr> <img src="https://analytics.click2apply.net/v/4eaAM1H4KwrqUo6zuV5nZ"> <p>PI115862848</p>

Categories

Posted: 2019-11-27 Expires: 2019-12-28

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Research Nurse

Dartmouth College
Hanover, NH 03755

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast