- Provide research support to multiple principal investigators and project coordinators who are members of the Wilmot Cancer Prevention and Control Research program.
- Provides support for studies conducted at various Wilmot Cancer Institute (WCI) locations across the catchment area.
- Screen and identify potential study patients by participating in multidisciplinary clinics, reviewing clinic schedules, using MyChart, collaborating with CTSI, developing and disseminating marketing materials, and developing new effective methods for recruitment.
- Identify and provide for scheduling of study events for patients enrolled.
- Schedule all patient study visits both face-to-face and electronic (e.g. Telemedicine, Zoom)
- Maintain patient data such as consent forms, letters, and appointment notices.
- Collect clinical data during all phases of care while patient is on study, i.e., medical record review, functional data, biological data; complete case report forms
- Assist with collection of biological and physiological data/samples and delivery to labs and basic processing
- Learn and administer new assessment techniques for study visits
- Review and evaluate patient data for statistical analysis and perform simple statistical analyses as needed
- Monitor studies regularly for conformity with Unit, Cancer Center, University and CTO (Clinical Trials Office) standard operating procedures and verify data ensuring compliance with requirements of
- Serve as point of contact for patients concerning study matters within the Wilmot Cancer Institute's on- and off-site locations. Maintain and prepare detailed documentation of treatment and follow-up of enrolled patients. Update documentation of patient procedures or data as they occur.
- Coordinate appointments and correspondence with patients participating in studies.
- Collaborate with personnel in other departments and at other Wilmot locations to implement patient activities.
- Consult regularly with physicians and other health care professionals involved with patients enrolled in studies
- Participate in the preparation of study documents and regulatory approvals.
- Review and/or edits study documents.
- Manage regulatory documents for the duration of studies.
- Organize documents for local audits.
- Assist with data analysis and preparation of materials for publication. Prepare and collate patient study information, status reports and updates as necessary for reporting on progress of patients enrolled in studies in order to accomplish a timely completion.
- Bachelor's degree in health-related, social science or appropriate field.
- 2-3 years of clinical research of relevant work experience or equivalent combination of education and experience.
- Excellent communication and organizational skills; attention to detail and problem-solving skills are essential.
- Ability to handle several projects simultaneously, prioritize and shift priorities quickly.
- Possess a high degree of self-motivation. Knowledge of computer databases, MS Office (e.g. Word, Excel, and PowerPoint), REDCap, OnCore, Zoom, Microsoft Teams, email, internet, and graphics packages are important.
- Requires reliable/efficient transportation for travel to off-site locations.
- Careers
- Sign In
- New User
-
Clinical Research Spec II
3 weeks ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours Range URG 108 Cancer Center/Clin Trials Ofc · Schedule · 8 AM-5 PM · Responsibilities · GENERAL PURPOSE: · The Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the planning, coordinat ...
-
Sr Clinical Research Spec
3 weeks ago
The University of Rochester Rochester, United StatesWe are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our dynamic team focused on advancing health equity for older adults with cancer. The Senior Research Coordinator will play a pivotal role in the execution Clinical Research, Clinical, R ...
-
Sr Clinical Research Spec
21 hours ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours Range URG 110 Surgery-Cancer Control · Schedule · 8 AM-4:30 PM · Responsibilities · GENERAL PURPOSE: · This position is an experienced Clinical Research Professional responsible for providing leadership in planning, implementing, monitoring, and evalu ...
-
Clinical Research Spec II
3 weeks ago
The University of Rochester Rochester, United StatesThe Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Under the ul Clinical Research, Clinical, ...
-
Clinical Research Spec II
3 days ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · The Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Under the ultimate resp ...
-
Sr Clinical Research Spec
3 weeks ago
The University of Rochester Rochester, United StatesThis position is an experienced Clinical Research Professional responsible for providing leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols. Under the ultimate responsibility of the Principal Investi Clinical Research, Clinical, ...
-
Sr Clinical Research Spec
21 hours ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · We are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our dynamic team focused on advancing health equity for older adults with cancer. The Senior Research Coordinator will play a pivotal role in the execution and managem ...
-
Sr Clinical Research Spec
3 days ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours Range URG 110 Surgery-Cancer Control · Schedule · 8 AM-5 PM · Responsibilities · GENERAL PURPOSE: · We are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our dynamic team focused on advancing health equity for o ...
-
Human Subject Research Spec I
5 days ago
The University of Rochester Rochester, United StatesHuman Subject Research Spec I Next Job Apply for Job When you are ready to apply, registering only takes a minute. Your online account allows you to upload your resume or CV, apply for jobs and access our online career tools. For general questions ab Research, Technology, Educati ...
-
Human Subject Research Spec I
2 days ago
University of Rochester Rochester, United StatesHuman Subject Research Spec I · Next Job · Apply for Job · When you are ready to apply, registering only takes a minute. Your online account allows you to upload your · resume or CV, apply for jobs and access our online career tools. · For · general questions about the online app ...
-
Human Subject Research Spec I
2 days ago
The University of Rochester Rochester, United States: - - Work daily on large community-based pediatric asthma interventions within the city of Rochester. Recruit participants into interventions and ensure timely follow-up data collection. Explain studies in detail, use own judgment to answer particip Research, Microsoft, Data Ent ...
-
Human Subject Research Spec I
21 hours ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours Range URG 106 General Pediatrics · Position ends July 31, 2024 · Strong Candidate Identified · Position ends July 31, 2024 · Schedule · 11 AM - 2 PM; WKNDS; NO HOLIDAYS, EVENINGS AND WKNDS REQUIRED; SCHEDULE VARIES BASED ON OPERATIONAL NEEDS. · How To ...
-
Human Subject Research Spec I
3 weeks ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours Grade 051 General Pediatrics · End Date: December 31, 2025; with possible renewal pending grant funding · Schedule · 8:30 AM-5 PM; WKNDS; NO HOLIDAYS, EVENINGS AND WKNDS REQUIRED; SCHEDULE VARIES BASED ON OPERATIONAL NEEDS. · Responsibilities · End Da ...
-
Human Subject Research Spec I
3 days ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · Coordinates the activities associated with human subject research. · **RESPONSIBILITIES:** · + Coordinates the administrative details required to initiate and conduct human subject research, including receiving, distributing and explaining study information, su ...
-
Sr Human Subject Research Spec
3 weeks ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · Under the direction of the Research Manager, with latitude for independent judgement, this individual will have the responsibility for managing clinical research trials, from industry, NIH, foundations and internal funds. This individual will oversee the day to ...
-
Clinical Research Data Spec I
3 weeks ago
The University of Rochester Rochester, United StatesUnder the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating proced Clinical Research, Clinical, ...
-
Human Subject Research Spec I
3 days ago
University of Rochester Rochester, United StatesResponsibilities · **End Date: December 31, 2025; with possible renewal pending grant funding** · **Position Summary** **:** · Work daily on large community-based pediatric asthma interventions within the city of Rochester. Recruit participants into interventions and ensure timel ...
-
Human Subject Research Spec I
3 weeks ago
University of Rochester Rochester, United StatesResponsibilities · **Position Summary:** · Coordinates the activities associated with human subject research. · **Responsibilities:** · + Coordinates the administrative details required to initiate and conduct human subject research, including receiving, distributing and explaini ...
-
Human Subject Research Spec I
2 days ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · Coordinates the activities associated with human subject research. This person will be responsible for recruitment and have administrative responsibilities, including screening and recruiting subjects, performing informed consenting and interviews, completing d ...
-
Human Subject Research Spec I
3 days ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · Coordinates the activities associated with human subject research. · **JOB DUTIES AND RESPONSIBILITIES:** · 1. Coordinates the administrative details required to initiate and conduct human subject research, including receiving, distributing and explaining study ...
Sr Clinical Research Spec - Rochester, United States - University of Rochester
![Default job background](https://contents.bebee.com/public/img/bg-user-ex-1.jpg)
Description
GENERAL PURPOSE:
This position is an experienced Clinical Research Professional responsible for providing leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols.
Under the ultimate responsibility of the Principal Investigator (PI) and/or leadership of the clinical trial, the individual in this position will have responsibilities for managing multiple studies' including day-to-day operations, carry out all study coordination duties from protocol development and initiation to study close-out according to regulatory/sponsor guidelines, and ensure each study's integrity.
The individual in this role will monitor and maximize adherence to research standards, regulatory guidelines, and approved operational procedures; work closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to study protocol; manage study-related administrative and human resources tasks; and facilitate across-the-board flow of information, orchestrating study activities and personnel.
The coordinators in this role will also be responsible for assisting in developing capacity and accruing participants across the entire Wilmot catchment area.
JOB DUTIES AND RESPONSIBILITIES:
Coordinate local clinical research projects
Study Documentation and Correspondence
Regulatory Responsibilities
Study Analysis
QUALIFICATIONS:
Required:
Preferred:
The University of Rochester is committed to fostering, cultivating, and preserving a culture of equity, diversity, and inclusion to advance the University's mission to Learn, Discover, Heal, Create - and Make the World Ever Better.
In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion/creed, sex, sexual orientation, citizenship status, or any other status protected by law.
This commitment extends to the administration of our policies, admissions, employment, access, and recruitment of candidates from underrepresented populations, veterans, and persons with disabilities consistent with these values and government contractor Affirmative Action obligations.
How To Apply
All applicants must apply online.
_EOE Minorities/Females/Protected Veterans/Disabled_
Pay Range
Pay Range:
$ 59,197 - $ 82,888 Annually
_The referenced pay range represents the minimum and maximum compensation for this job.
Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
_Apply for Job
Location: School of Medicine & Dentistry
Full/Part Time: Full-Time
Opening:
Schedule: