Bethlehem, Pennsylvania
Denver, Colorado
Minnesota
Bloomington, Indiana
Indianapolis, Indiana
Hialeah, Florida
Phillipsburg, New Jersey
Hershey, Pennsylvania
Hershey, Pennsylvania
Arkansas
Posted: 24-Jan-25
Location: Dallas, Texas
Categories:
Internal Number: 24015079-1
Research Project Coordinator (Study Start Up)
Location: Dallas
Specialty: Oncology Research
Hours of operations: 8:00 am - 4:30 pm
***The Research Project Coordinator for Oncology Research will facilitate and oversee study startup steps at the site level for oncology clinical trials. This includes site feasibility, handling initial essential documents, and liaison with investigators/site staff/various departments from receipt of the study until site activation. Review potential studies to confirm their fit with the site portfolio and work closely with the contracts, budget development, and regulatory team. Routinely collect and assess startup metrics to identify opportunities for startup timeline improvement. Provide clinical trial education in preparation for transition from the startup team to the clinical team, ensuring a smooth handoff. Two years of Clinical Research Coordinator experience, Projects experience is a plus.***
JOB SUMMARY
The Research Project Coordinator is accountable for planning, developing, implementing, managing and reporting on multiple aspects of a multidisciplinary research program. This position will use project management skills and tools to develop and implement strategies that ensure timely advancement of a proposed research program to meet intended goals and priorities while complying with all institutional, federal and state rules, regulations and funding constraints.
ESSENTIAL FUNCTIONS OF THE ROLE
- Works with team managers and others to define the strategic initiatives, scope, goals and timelines of the research program.
- Develops program budgets and ensures that budget requirements are met, including review of program-related contracts and approval of invoices within the program budget.
- Prepares helping documents, including the clinical protocol, investigator's brochure, case report forms, informed consent documents and components of an IND application.
- Serves as the program's liaison with internal and external departments and personnel involved in, or contributing to, the program to resolve barriers to the advancement of the program's strategic initiatives. Uses project management skills to ensure that the program progresses according to established timelines.
- Fosters relationships with external entities, including academia, pharmaceutical and biotechnology industries; maintains current relationships and establishes new relationships with entities that can contribute to the goals of the program.
- Designs and implements processes and procedures to ensure advancement of the program's strategic initiatives.
- Provides guidance to program team members and interacts regularly with the program team to establish resource needs, coordinate activities of operational areas and identify deliverables and target due dates.
- Organizes and conducts team meetings to ensure adherence to strategic initiatives, goals, budget and timelines.
KEY SUCCESS FACTORS
- Proven written and oral communication skills.
- Proven leadership skills in project management, including project management tools and techniques.
- Exceptional computer skills, including Microsoft office, Excel and PowerPoint.
- Ability to manage time reactive projects in order to meet deadlines.
- Exceptional ability to establish and maintain effective working relationships.
BENEFITS
Our competitive benefits package includes the following.
- Immediate eligibility for health and welfare benefits
- 401(k) savings plan with dollar-for-dollar match up to 5%
- Tuition Reimbursement
- PTO accrual beginning Day 1
Note: Benefits may vary based upon position type and/or level
QUALIFICATIONS- EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification
- EXPERIENCE - 2 Years of Experience