Bausch Health - Lansing, MI

posted 2 months ago

Full-time - Mid Level
Lansing, MI
10,001+ employees
Chemical Manufacturing

About the position

Bausch + Lomb is seeking a Manager for Clinical Trials in Ophthalmology to lead and oversee clinical trial activities. This role is pivotal in ensuring that clinical trials are conducted in compliance with FDA regulations and company standard operating procedures. The Manager will be responsible for a variety of tasks prior to the commencement of clinical trials, including clinical planning, protocol development, and site selection. This position requires effective communication with clinical trial sites and vendors to manage logistics, contract agreements, and training materials. The Manager will also provide clinical oversight during trials, ensuring adherence to Good Clinical Practices (GCP) and regulatory requirements. In addition to overseeing trial conduct, the Manager will collaborate on clinical data processing and assist in the evaluation and analysis of clinical trial data. This includes generating Data Clarification Forms for any missing or inaccurate data and ensuring that all changes are accurately captured in the database. The role also involves writing clinical reports, preparing documentation for FDA submissions, and tracking study-specific payments. The Manager will work closely with various departments, including Clinical Operations, Research and Development, and Regulatory Affairs, to ensure that all systems and procedures are efficiently completed. The position requires strong analytical skills, the ability to interpret medical literature, and excellent verbal and written communication skills. The Manager will also be responsible for conducting presentations on clinical information and collaborating on technical writing projects such as white papers and manuscripts. This role is essential for facilitating cooperation among internal and external stakeholders and ensuring the successful execution of clinical trials.

Responsibilities

  • Leads or collaborates on required tasks prior to commencement of clinical trials including clinical planning, protocol development, and IRB submissions.
  • Provides clinical oversight and management for clinical trials to ensure compliance with FDA and international regulatory requirements.
  • Communicates with vendors and clinical trial sites regarding study conduct and logistical management.
  • Collaborates on clinical data processing in accordance with departmental SOPs and guidelines.
  • Verifies, reviews, and tracks CRFs and generates Data Clarification Forms for missing or inaccurate data.
  • Assists in the evaluation and analysis of clinical trial data and completion of reporting requirements.
  • Tracks study specific payments and provides operational support for departmental systems.
  • Collaborates on project teams with Clinical Operations, Research and Development, and other departments.
  • Leads or collaborates on technical writing projects including white papers and manuscripts.
  • Acts as a liaison between internal and external stakeholders to facilitate cooperation.
  • Conducts presentations of clinical information concerning specific projects.

Requirements

  • Bachelor's degree in a health profession or science.
  • Minimum 5 years of ongoing clinical trials experience in the pharmaceutical or device industry.
  • Demonstrated proficiency in knowledge of GCPs and FDA regulatory requirements.
  • Knowledge of medical terminology.
  • Ability to effectively work independently.
  • Excellent verbal and written communication skills plus computer proficiency (Word, Excel, Outlook) and data management experience.

Benefits

  • Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date
  • 401K Plan with company match and ongoing company contribution
  • Paid time off - vacation (3 weeks - prorated upon hire), floating holidays and sick time
  • Employee Stock Purchase Plan with company match
  • Employee Incentive Bonus
  • Tuition Reimbursement (select degrees)
  • Ongoing performance feedback and annual compensation review
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