Long term opportunity for a Senior Electrical Engineer with a great pharmaceutical company!
Job Detail
Job Description
Responsibilities:
- Overseeing the planning, implementation, and management of clinical trials, ensuring that they are conducted in compliance with regulatory and ethical guidelines
- Developing study protocols, case report forms, and other study-related documents in collaboration with cross-functional teams
- Identifying and managing vendors, including contract research organizations (CROs), clinical laboratories, and other service providers
- Monitoring study progress, including patient enrollment, data collection, and analysis
- Ensuring timely data entry and query resolution, and managing data cleaning and database lock activities
- Managing study budgets and timelines, and ensuring that study costs are within budget
- Maintaining strong relationships with key stakeholders, including investigators, study coordinators, and regulatory authorities
- Participating in the preparation of regulatory submissions and inspections
- Providing guidance and mentorship to clinical operations staff as needed
Requirements:
- Bachelor's or advanced degree in a life sciences field
- Minimum of [insert number of years] years of experience in clinical trial management or related field
- Knowledge of ICH-GCP guidelines and other regulatory requirements for clinical trials
- Strong project management skills, including the ability to manage timelines, budgets, and resources effectively
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders
- Strong analytical skills, with the ability to analyze complex data sets and draw insights
- Ability to work independently and take initiative to resolve issues and ensure timely study execution
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