Assistant Director for Clinical Trials

Stony Brook Medicine

$100K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree or higher in a related field
  • 3 years of experience in clinical research, including 2 years with sponsored trials
  • Supervisory experience over research coordinators
  • Experience with research protocols, budget preparation, and sponsor negotiations
  • Preferred: Master's degree and 4+ years in clinical research, fluent in Spanish

Responsibilities

  • Direct day-to-day operations of the Clinical Research Core
  • Develop and manage financial policies and procedures
  • Supervise, train, and mentor research staff
  • Facilitate study startup including budget and contract negotiations
  • Manage financial aspects of industry-funded clinical trials
  • Oversee regulatory compliance for research studies
  • Prepare documents for presentations and sponsor audits

Benefits

  • Opportunity for professional development and mentoring
  • Access to collaborative resources across SUNY campuses
  • Engagement with diverse clinical research projects
  • Working with an experienced and supportive team
  • Contribution to significant research initiatives at Stony Brook
Full Job Description
Required Qualifications (as evidenced by an attached resume):
Bachelor's degree (foreign equivalent or higher) plus three (3) years of full-time experience in clinical research with two (2) years of this working with sponsored clinical trials. Administrative and managerial experience working with research projects and clinical trials involving an external sponsor. Supervisory experience to include supervising research coordinators. Experience working with research protocols and budget preparation and negotiation with the sponsor.

Preferred Qualifications:
Master's degree (foreign equivalent or higher). Four (4) or more years of full-time experience in clinical research involving sponsored clinical trials. Proficient in ONCOR Clinical Trials Management System. Bilingual in Spanish.

Brief Description of Duties:
The incumbent directs the day-to-day operations of the Clinical Research Core, developing, managing, and evaluating all administrative and financial policies and procedures of the office. Responsible for developing position descriptions, hiring, training, supervising, performing yearly reviews, etc. Provides expertise, training, and mentoring to research staff, not limited to Investigators and Study Coordinators. Facilitates study start up (budget development, contract negotiation, administrative approvals, etc.), as well as manages financial aspects of industry funded clinical trials for a number of departments within the SOM. Establishes collaborative processes and shared resources among other SUNY campuses with the goal of identifying common needs. Reports directly to the Associate Director for Clinical Trials at Stony Brook School of Medicine.

Duties:

Staff/Personnel Responsibilities:
• Supervises CRC staff, providing specific work assignments to staff in order to facilitate research at SBU, performing QA on assigned work, carrying out performance programs reviews and evaluations, managing time off requests, etc.
• Ensure that policies and procedures are adhered to.
• Trains and mentors' staff (PI's, department administrators, Study Coordinators, etc.) on research-related practices.
• Facilitates educational research training to study coordinators throughout the year.

Financial Responsibilities:
• Budget development and negotiation for industry-funded clinical trials for SOM.
• Payment Terms negotiation with sponsors.
• Management of Clinical Conductor Clinical Trails Management System (CTMS). Creation of new studies and their negotiated budget
• Training of Study Coordinators on the use of the CTMS.
• Provide technical support to users of CTMS.
• Run monthly financial reports and queries for data entry.
• Study invoicing, payments, accounts reconciliation, and closeout.

Other:
• Oversees regulatory aspects of studies, such as IRB submission and ClinicalTrials.gov entries for research compliance.
• Day-to-Day study coordination, including patient recruitment and consent, study visits, collection, preparation, shipping of human samples, and data entry.
• Preparation of necessary documents, figures, and tables for research presentations, Data and Safety Monitoring Board meetings, and sponsor audits.

Other Duties as assigned

Special Notes:
The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Exempt position, not eligible for the overtime provisions of the FLSA. Minimum salary threshold must be met to maintain FLSA exemption.

Essential Position:This has been designated as an essential position based on the duties of the job and the functions performed. Positions that are designated as such may be required to report to work/remain at work even if classes are canceled, and the campus is working on limited operations in an emergency.

For this position, we are unable to sponsor candidates for work visas.

Resume/CV and cover letter should be included with the online application.

The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU's good faith and reasonable estimate of the range of possible compensation at the time of posting.

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