Position Details
Position Information
Recruitment/Posting Title |
Research Associate III |
Job Category |
Staff & Executive - Research (Laboratory/Non-Laboratory) |
Department |
RWJ-Medicine-Cardiology 5-Meb |
Overview |
New Jersey's academic health center, Rutgers Biomedical and Health Sciences (
RBHS) takes an integrated approach to educating students, providing clinical care, and conducting research, all with the goal of improving human health. Aligned with Rutgers University-New Brunswick and collaborating university wide,
RBHS includes eight schools, a behavioral health network, and six centers and institutes that focus on cancer treatment and research, neuroscience, clinical and translational research, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research.
Our faculty are teachers, clinicians, and scientists with unparalleled experience who advance medical innovation and provide patient care informed by the latest research findings. We offer an outstanding education in medicine, dentistry, pharmacy, public health, nursing, biomedical research, and the full spectrum of allied health careers.
Our clinical and academic facilities are located throughout the state including New Brunswick, Piscataway, Newark, Scotch Plains, Somerset, Blackwood, and other locations. Clinical partners include Robert Wood Johnson University Hospital in New Brunswick, University Hospital in Newark, and other affiliates.
Through this community of healers, scientists, and scholars, Rutgers is equipped as never before to transform lives. |
Posting Summary |
Rutgers, The State University of New Jersey, is seeking a Research Associate
III for the department of Medicine at the Robert Wood Johnson Medical School.
The Clinical Research Associate
III, under the direct supervision of the Research Director of the Division, will assist in activities to support and grow the Clinical Research in the Division. These activities include, but may not be limited to supporting lab testing, including setup, processing and shipping, ordering of supplies, developing source documents, data entry, record maintenance and archiving, study visit tracking, assisting with budget preparation and registration of study subjects.
IRB submission and maintaining compliance with
IRB,
HIPAA, and
FERPA guidelines, and engaging scientifically in grant applications.
Among the key duties of this position are the following:
- Works closely with research director and principal investigator(s) to develop protocols for clinical research proposals, organize research activities and maintain effective communication between project staff, external collaborators, funding agencies, and regulatory entities.
- Follows protocol guidelines in the collection of clinical data and/or administration of clinical tests. Coordinate, implement and manage procedures to collect data from patient charts, medical records, prescreening interviews, questionnaires, diagnostic tests and other sources. Ensure compliance with protocol guidelines and requirements of regulatory agencies (such as IRB, HIPAA, and FERPA guidelines); identify problems and/or inconsistencies and monitor patient progress to include documentation and reporting of adverse events; recommend corrective action as appropriate.
- Assists with and oversee ongoing research studies based on the research protocols, including subject recruitment, data collection, database entry and management, statistical analysis and administrative duties.
- Oversees consenting activities, maintain study databases at the highest level of completeness and accuracy, and safeguard the safety and the right to privacy for study participants.
- Maintains documents required for the regulatory binder, investigative drug binder and any other document repositories required by the principal investigator, or regulatory entities.
- Assists in grant preparation, submission deadlines, and lab organization.
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Position Status |
Full Time |
Hours Per Week |
|
Daily Work Shift |
|
Work Arrangement |
This position requires a fully on-site work arrangement. |
FLSA |
Exempt |
Grade |
18S |
Position Salary |
|
Annual Minimum Salary |
51169.00 |
Annual Mid Range Salary |
60954.00 |
Annual Maximum Salary |
71835.00 |
Standard Hours |
37.50 |
Union Description |
HPAE 5094 |
Payroll Designation |
PeopleSoft |
Benefits |
Rutgers offers a comprehensive benefit program to eligible employees. For details, please go to
http://uhr.rutgers.edu/benefits/benefits-overview.
|
Seniority Unit |
|
Terms of Appointment |
Staff - 12 month |
Position Pension Eligibility |
ABP |
Qualifications
Minimum Education and Experience |
- Master's Degree in a relevant science (e.g. biological sciences, biomedical engineering, public health) plus one (1) year of related research experience, or a Bachelor's Degree in a relevant science (e.g. biological sciences, biomedical engineering, public health) plus two (2) years of related research experience.
|
Certifications/Licenses |
|
Required Knowledge, Skills, and Abilities |
- Must be computer literate with proficiency and working knowledge of database and reporting tools such as Microsoft Word, Excel and PowerPoint.
- Must be capable of independent decision-making, and multitasking.
- To be successful, the candidate must have excellent organization, communication and interpersonal skills.
|
Preferred Qualifications |
- Understanding of the software program Oncology Collaborative Research Environment (Oncore).
- Experience with electronic medical record management systems (Epic/SCM).
|
Equipment Utilized |
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Physical Demands and Work Environment |
- Physical Demands: Standing, sitting, walking, talking or hearing. No special vision requirements.
- Work Environment: Office environment. Moderate Noise.
|
Special Conditions |
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Posting Details
Posting Number |
24ST1594 |
Posting Open Date |
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Special Instructions to Applicants |
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Regional Campus |
Rutgers Biomedical and Health Sciences (RBHS) |
Home Location Campus |
Downtown New Brunswick |
City |
New Brunswick |
State |
NJ |
Location Details |
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Pre-employment Screenings
All offers of employment are contingent upon successful completion of all pre-employment screenings.
Immunization Requirements
Under Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption. Additional infection control and safety policies may apply. Prospective employees should speak with their hiring manager to determine which policies apply to the role or position for which they are applying. Failure to provide proof of vaccination for any required vaccines or obtain a medical or religious exemption from the University will result in rescission of a candidate's offer of employment or disciplinary action up to and including termination.
Affirmative Action/Equal Employment Opportunity Statement
It is university policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, affectional or sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As an institution, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment. For additional information please see the Non-Discrimination Statement at the following web address: http://uhr.rutgers.edu/non-discrimination-statement
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