Position Details
Position Information
Recruitment/Posting Title |
Research Teaching Specialist II |
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 five centers and institutes that focus on cancer treatment and research, neuroscience, 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-at Rutgers University-New Brunswick, including Piscataway; and at locations in Newark, Scotch Plains, Somerset, Stratford, and other locations. Clinical partners include Robert Wood Johnson University Hospital in New Brunswick, Newark's 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 Teaching Specialist II for the department of Medicine at the Robert Wood Johnson Medical School.
The primary role of this position, under the direction of the Principal Investigators and Division's Research Director, is to manage daily clinical and other research activities and to function as the primary contact for various external collaborators, and interinstitutional departments to ensure compliance with institutional, federal, and state regulatory agencies. These activities include but may not be limited to preparation of documents for submission to the Institutional Review Board (
IRB), Investigational New Drug/Device (
IND/
IDE) preparation and maintenance, submissions of letters of intent and protocols to be submitted to external IRBs. They will manage and maintain regulatory documents for the
CRU, investigator-initiated, cooperative groups and industry trials. This position will assist in developing and maintaining Standard Operating Procedures (SOPs), training personnel in research, that comply with all pertinent regulations to ensure the accuracy and timely completion of all protocols, consent forms, amendments, annual re-approvals, serious adverse events, and
IND/
IDE safety reports to the
IRB.
Among the key duties of this position are the following:
- Serves as primary point of contact with internal and external collaborators including the sponsor, clinical research organization, institutional review board, principal investigator and the study team.
- Communicates and collaborates specific study requirements to the research team, including internal and external parties, sponsor, monitors, and PI or investigators.
- Performs and manages multiple research and technical operations independently or as assigned (including preparing, compiling and coordinating regulatory document submission for pharmaceutical and clinical research organization, IRB correspondence, ensuring data quality by performing regular audits according to Standard Operating Procedures with high precision) followed by appropriate reports, recommendations and conclusions.
- Assists with the preparation of proposals, formal applications and justifications for grant applications.
- Develops recommendations regarding budget proposals for the research projects and actively work with finance team to generate and reconcile invoices for study-related payments. Assists in the establishments of performance standards including regulatory compliance as well as to write and/or maintain standard operating procedures, department working practices ensuring FDA commitments are met and are as per standard medical practices from study start-up till close-out.
- Assists with the instructing and training of clinical research coordinators, research assistants, and fellows to develop the skills necessary on adherence to compliance policies and procedures in research.
|
Position Status |
Full Time |
Hours Per Week |
|
Daily Work Shift |
|
Work Arrangement |
This position requires a fully on-site work arrangement. |
FLSA |
Exempt |
Grade |
25S |
Position Salary |
|
Annual Minimum Salary |
70041.00 |
Annual Mid Range Salary |
84083.00 |
Annual Maximum Salary |
99858.00 |
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 plus two (2) years of related regulatory research experience, or a Bachelor's Degree in a relevant science plus three (3) years of related research experience required.
|
Certifications/Licenses |
- Association of Clinical Research Profession (ACRP), SOCRA or other research certification (or willingness to obtain within 1 year of hire) required.
|
Required Knowledge, Skills, and Abilities |
- Excellent written and verbal communication skills with ability to manage independent projects and meet deadlines.
- Excellent organizational and communication skills required.
- Demonstrated computer skills with Microsoft Office applications.
- Strong analytical skills and the ability to think creatively with excellent leadership skills.
- Proficiency with Internet applications and in using various Microsoft Office applications such as Word, Excel, Power Point and Outlook.
- Excellent interpersonal, writing, and verbal communication skills.
- Ability to interface effectively with all levels of management.
- Must work and communicate effectively with both internal and external team members.
- Strong organizational and time management skills and ability to multitask and work well under pressure.
- Ability to identify, analyze and solve problems.
|
Preferred Qualifications |
- Bilingual skills in Spanish.
|
Equipment Utilized |
|
Physical Demands and Work Environment |
- Physical Demands: Attending meetings and regular computer use requires sitting and using hands to finger, handle or feel over 2/3 of the time. Due to the location of our clinical facilities, standing and walking can be expected up to 2/3 of the time. Typing and writing requires reaching with hands and arms up to 2/3 of the time. Lifting medical records, case report forms and laboratory supplies can require lifting up to 50 lbs. in addition to stooping, kneeling or crouching for such materials 1/3 of the time.
- Work Environment: Office environment with moderate noise.
|
Special Conditions |
|
Posting Details
Posting Number |
25ST0512 |
Posting Open Date |
|
Special Instructions to Applicants |
|
Regional Campus |
Rutgers Biomedical and Health Sciences (RBHS) |
Home Location Campus |
Downtown New Brunswick |
City |
New Brunswick |
State |
NJ |
Location Details |
|
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
|