LOCATION:
Monday – Friday / On-site / Irving, TX
COMPANY OVERVIEW: Alliance Clinical Network we’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research. We bring our energy and our passion to improving patient lives every day.
SUMMARY: The Clinical Project Coordinator will support the planning, execution, and monitoring of clinical research projects across our site network. This role involves coordinating with various stakeholders, ensuring compliance with regulatory requirements, and maintaining project timelines. The ideal candidate will have strong organizational skills, attention to detail, and a passion for clinical research.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Review and assess clinical trial protocols to understand the study requirements, objectives, and timelines
- Assist in the development and implementation of project plans, including timelines, milestones, and deliverables.
- Coordinate with site staff, investigators, and external partners to ensure smooth project execution.
- Monitor project progress and provide regular updates to senior management.
- Ensure compliance with all regulatory requirements and company policies.
- Manage project documentation, including protocols, consent forms, and regulatory submissions.
- Identify and resolve project-related issues and risks.
- Support the preparation of project budgets and track expenses.
- Facilitate communication between project stakeholders to ensure alignment and collaboration.
- Participate in project meetings and provide administrative support as needed.
QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION AND EXPREIENCE:
- Bachelor’s degree in a related field (e.g., Life Sciences, Public Health).
- 1-2 years of experience in clinical research or project management.
- Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
- Strong organizational and time management skills.
- Excellent communication and interpersonal skills.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work independently and as part of a team.
- Detail-oriented with a proactive approach to problem-solving.
Preferred Qualifications:
- Experience with clinical trial management systems (CTMS).
- Certification in project management (e.g., PMP, CAPM).
- Familiarity with electronic data capture (EDC) systems.
- Familiarity with project plans
BENEFITS:
- 401 (k) Retirement Plan
- Medical, Dental, and Vision Insurance
- Paid Time Off (PTO)
- Floating Holidays
And more!