Employer Industry: Medical Device Manufacturing

Why consider this job opportunity:
- Salary up to $248,340
- Comprehensive benefits package including medical, dental, and vision coverage
- Generous 401k matching and tuition reimbursement programs
- Opportunities for career advancement and professional development
- Engaging work environment with a focus on wellness, leadership development, and diversity
- Chance to contribute to innovative solutions in chronic pain treatment

What to Expect (Job Responsibilities):
- Define clinical research strategies, goals, and objectives for various clinical studies
- Collaborate cross-functionally to implement clinical study plans involving regulatory affairs, marketing, and research & development
- Manage a team of clinical scientists to work with physicians on study design and implementation
- Develop and approve protocols for both sponsored and investigator-initiated projects
- Prepare clinical reports for regulatory and medical purposes, including presentations and publications

What is Required (Qualifications):
- Degree in science, health, or engineering (e.g., Electrical, Mechanical, or Biomedical Engineering) required; Master’s degree or PhD preferred
- Minimum of 5 years of experience in clinical/scientific research and medical device/pharmaceutical clinical trials
- At least 5 years of experience working with clinical professionals in a cross-functional product development environment
- Strong understanding of clinical trial methodologies and regulatory requirements (e.g., FDA, EMA)
- Proven ability to lead and motivate cross-functional teams

How to Stand Out (Preferred Qualifications):
- Experience in clinical trial design and implementation
- Familiarity with ICH-GCP guidelines governing clinical trials
- Strong stakeholder communication skills for liaising with various teams and external partners
- Expertise in resource allocation for optimizing trial outcomes
- Ability to adapt strategies in response to changing conditions

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