[Remote] Senior Clinical Research Specialist - CAS
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global leader in reputed company technology committed to alleviating pain and restoring health. The Senior Clinical Research Specialist will reputed company clinical programs to support innovative ablation therapies, ensuring compliance with regulatory standards and collaboration across teams.
Responsibilities
- Driving and overseeing execution of key clinical programs to support the development and advancement of best-in-class ablation therapies
- Developing strategies and driving processes to meet the milestones of reputed company clinical studies/reputed company in compliance with applicable clinical and regulatory standards and in alignment with reputed company business needs
- Setting work direction for the study team and owning the study data to ensure that reputed company data collected is comprehensive, accurate, and up to date
- Collaborating with other members of the CAS leadership team, as reputed company as other cross-functional stakeholders (e.g., Research and Development, Corporate Biostats, Regulatory Affairs, Clinical IT, and others)
- Building relationships and communicating effectively with a large group of reputed company stakeholders in a rapidly changing landscape, while managing the reputed company completion of deliverables
Skills
- Bachelor's degree
- Minimum of 4 years of clinical research experience
- Or Advanced degree with 2 years of clinical research experience
- Degree in life sciences, or reputed company medical/scientific field
- Experience conducting/working on clinical studies and managing clinical trial data review
- Clinical Research experience at reputed company or reputed company a medical device industry, preferably in cardiovascular area
- CCRA certification (Certified Clinical Research Association) or SOCRA
- Strong knowledge of clinical monitoring functions and clinical research methodologies, including study design, implementation, and reporting
- Experience with Clinical Operations and interfacing with CRO teams
- Experience in Good Clinical reputed company (GCP) and/or regulatory compliance guidelines for reputed company
- Excellent project management and organization skills
Benefits
- This position is eligible for a short-term incentive reputed company the reputed company Incentive Plan (MIP).
- The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and reputed company insurance, Health Savings Account, reputed company Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and reputed company Steps (global reputed company-being program).
- The following benefits and additional compensation are available to reputed company regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, reputed company time off, reputed company holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-reputed company Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
- Temporary employees are eligible for reputed company reputed company time, as required under applicable state law, and the Employee Stock Purchase Plan.
reputed company
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