Manager, Clinical Research

Who We Are

At Panorama Eyecare company, we are not just a team; we are a community of dedicated professionals united in our quest to provide the best eyecare anywhere. Our unflinching commitment to excellence and our core values are what make us an Employer of Choice. Join us in shaping the future of eyecare as we thrive together!

The Position:

As the Manager, Clinical Research at Panorama Eyecare, you will play a pivotal role in our mission to deliver the best eyecare. You'll be part of a collaborative team that values Partnership, Engagement, Excellence, and Stewardship. Together, we create an environment where mutual respect is at the forefront, equipping you with the tools, training, and empowerment necessary to excel in your role.

The Role

The successful Manager, Clinical Research will contribute to the fulfillment of the Eye Center’s mission statement by providing patients with quality care and access to novel drugs and devices through clinical trials in which the Eye Center participates. This individual will ensure that Eye Center doctors are able to expand their practice as clinical trial investigators through the conduct of accurate and ethical studies. This individual must possess exceptional communication, leadership and research skills.

Major Responsibilities:

• Responsible for all study patient care including but not limited to: performing study related testing, consenting participants, dispensing study product, scheduling visits, completing source documentation, distributing stipends, and communicating with participants.
• Promotes clinical research studies and recruits patients to meet enrollment goals for each study.
• Manages research staff to ensure tasks are accomplished with efficiency, integrity, and in compliance with regulatory standards.
• Facilitates communication and maintains positive relationships between ECNC and all Sponsors, IRBs, and labs.
• Effectively communicates with other ECNC departments on study related matters.
• Maintains all study specific and ECNC required logs.
• Ensures protocol compliance in all aspects of study conduct.
• Attends periodic Investigator Meetings and research conferences.
• Negotiates budgets to ensure fair compensation for ECNC and study participants.
• Works with study monitors to complete queries and action items.
• Oversees IP accountability and maintenance.
• Reconciles all study payments with budgets.
• Creates source documentation that meets sponsor and regulatory standards.

Additional Responsibilities:

• Acquires skills necessary to perform each study.
• Thorough understanding of the purpose of the research, and ability to acquire information pertinent to each study.
• Demonstrates sound judgment in handling various situations that arise during a clinical trial.
• Effectively applies GCP in all aspects of clinical research.
• Works independently on tasks and delegates when appropriate.
• Trains ancillary research staff as needed.
• Ensures GCP/NIH certification is maintained for all research staff.
• Effectively prioritizes to ensure all tasks are completed in a timely manner.
• Accepts other duties as assigned.