As a Medical Project Coordinator, you will assist in the management and evaluation of medical projects within clinical research programs. Your role will focus on maintaining the consistency, alignment, and compliance of internal processes while ensuring the successful execution of projects through various stages of the project lifecycle.
Key Responsibilities:
- Safety Data Coordination:
- Review and coordinate safety data using line listings, dashboards, and visualization tools.
- Identify safety trends, ensure coding consistency, and resolve issues or escalate as necessary.
- Review and summarize data for safety review meetings and contribute to safety aggregate reports.
- Project Management:
- Help create and review safety and medical management plans to ensure they align with contracts.
- Coordinate project implementation, track metrics, and manage budgets.
- Monitor the status of data reviews, escalating any delays or risks to stakeholders.
- Participate in business development and strategy meetings as needed.
- Problem-Solving:
- Provide solutions for complex problems by evaluating various factors.
- Serve as a point of contact for clinical/data management project teams.
- Mentorship:
- Assist in training and mentoring junior team members.
Qualifications:
- Education: Undergraduate or graduate degree in a related field (Pharm D, PhD, BS in Science, RN, DDS, etc.).
- Experience: 2-5 years of experience in life sciences or medically related fields.
- Knowledge:
- Strong understanding of the clinical trials process and Good Clinical Practice (GCP).
- Background in the therapeutic area of clinical trials.
- Proficiency in safety data analysis, SAE processing, and drug development.
- Experience in risk assessment tools, biostatistics, and data management.
Skills:
- Strong problem-solving and critical thinking.
- Excellent oral and written communication.
- Ability to work collaboratively and handle challenges professionally.
- Attention to detail.
