Study Coordinator Salary at Pharmedge BETA

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POSITION RESPONSIBILITIES: Work with PI to develop study protocols and protocol amendments for the IRB as needed, including the development of new measures. Manage data collection, analysis and cleaning, performing regular audits to ensure that the data collected are complete and accurate, and that the research is being conducted as outlined in the protocol. Develop and manage REDCap database. Develop appropriate progress reports for the PI, study funding agency and the IRB. Assist PI with preparation of grant proposals (new and competing renewals). Assist the faculty in the in gathering the required documents and data needed to prepare grant applications. Secure related supporting letters and attachments required for grants and contracts. Confirm that the appropriate resources are available, which are needed by the PI. Arrange meetings of study partners, develop meeting agendas, and facilitate meeting Facilitate the preparation of conference abstracts, oral presentations, and poster p

POSITION RESPONSIBILITIES: Directly supervise approximately 9 staff members, including Study Coordinators, Medical Assistants, Interviewers, Phlebotomist, Clinician, etc. Supervise and oversee all aspects of research visits including recruitment, determination of eligibility, informed consent process, visit tracking, and follow-up. Collaborate with other members of the team as needed. Certify and train existing staff on new procedures, as well as assist in training newly hired staff. Regularly meet with research staff, faculty, lab personnel and other MWCCS employees. Conduct regular and annual skills trainings to ensure that all staff receive up-to-date training on relevant skills and procedures. Provide regular feedback to staff on performance, and additionally as needed. With the Project Director, responsible for providing any corrective action for staff as needed. Initiate and maintain all IRB protocols and activities with the Einstein and/or BRANY IRBs Collaborate with the Data Ma

POSITION RESPONSIBILITIES: Implement study protocols; Perform data collection and quality control of study data; Oversee the process by which participants are recruited into the study, adherence to research protocols in obtaining informed consent, blood drawing and testing, data collection and management and participant confidentiality; Develop and implement methods to track and follow-up with study participants; Assist with coordinating data safety monitoring and produce quarterly reports; Oversee questionnaires for completeness and accuracy; Arrange meetings of study partners, develop meeting agendas, and facilitate meeting; Implement quality control procedures; Assist in the preparation of grants for future studies; Develop and manage REDCap database. QUALIFICATIONS: Bachelors degree is required. Minimum Salary Range: USD $58,500.00/Yr. Maximum Salary Range: USD $58,500.00/Yr. About Us: This position is in the Division of Nephrology, with a primary assignment to the clinical studies

Job Details Job Location Jacobi - Bronx, NY Position Type Regular Full-Time Salary Range $75,000.00 - $75,000.00 Salary/year Job Shift 1 Job Category Administrative/Clerical Opportunity Details Physician Affiliate Group of New York (PAGNY) has an opportunity for aResearch CoordinatoratNYC Health + Hospitals/Jacobi and North Central Bronx. The Hospitals are part ofNYC Health + Hospitals.Jacobi is a 457-bed, Level I Trauma Center and NCB has 213 licensed beds.The hospital maintains a strong academic affiliation withAlbert Einstein Medical Collegeto maintain its high healthcare delivery standards. The mission ofNYC Health + Hospitalsis to extend equally to all New Yorkers, regardless of the ability to pay, comprehensive health services of the highest quality in an atmosphere of humane care, dignity, and respect. Their Values are built on a foundation of social and racial equity and has established the ICARE standards for all staff. NYC Health + Hospitalsis the nation's largest municipal h

COMPANY Volastra Therapeutics, Inc. is a clinical-stage oncology biotech company based in New York City, pioneering novel approaches to treating cancer by targeting chromosomal instability (CIN), a unique vulnerability in cancer. Since its founding in 2019, Volastra has grown to support ongoing discovery efforts and a growing clinical organization. Our lead pipeline programs focus on two distinct inhibitors of KIF18A, a novel therapeutic target. VLS-1488, internally discovered, entered clinical trials in Q4 2023 for the treatment of advanced cancers. Sovilnesib, in-licensed from Amgen in 2023, re-entered the clinic in Q2 2024. Both assets have been granted Fast-Track Designation by the FDA. Volastra is backed by top US and European venture firms such as Arch, Polaris, Vida, Droia, Catalio, and B Capital, alongside strategic investment from Eli Lilly. In addition to venture funding, Volastra has established partnerships with oncology leaders. Our senior leadership team is highly experie

JOB SUMMARY The Pharmacy Technician is responsible for supporting the Pharmacists by reviewing protocols and source documentation, handling drug preparation and dispensing doses during clinical trials as required. RESPONSIBILITIES Reviewing protocols and relevant source documents for study execution Performing pharmacy support services for clinical investigations Handling all drug preparation for clinical trials as needed Dispensing investigational products for clinical use as designated Completing drug accountability logs and ensuring source documentation is accurate Works under the supervisor of the Pharmacy Manager Works with site pharmacists, sponsors, business unit management, Principal Investigators, Sub Investigators, Clinicians, Project Managers and Study Coordinators Assist with handling schedule II - V drugs Assists with the extemporaneous drug preparation, under proper supervision Attend study team meetings to discuss study specific pharmacy requirements Other duties as assi

About Mirimus: Mirimus specializes in harnessing the power of RNA interference (RNAi) and CRISPR/Cas9 genome editing for cell and animal model creation for pre-clinical therapeutic development. Mirimus generates unique comparative gene-edited models for large pharma drug discovery groups and CROs. Mirimus is partnered with Charles River Laboratories and performs all of their custom mouse model creation for their North America GEMS division. Mirimus is also partnered with Biogen to develop novel RNAi therapeutics. Our mission is to provide superior preclinical models for target discovery and validation to accelerate therapeutic development for human health issues. About the Role: Mirimus is seeking a highly motivated, innovative and experienced full-time technician to contribute to their Genetically Engineering Service (GES) in the production of Animal Models and completion of research studies. Successful candidates will be part of an innovative and creative team with the opportunity to