Clinical Trials Operations Specialist

Bausch + Lomb; Juneau (AK); On-site; USD 85,000 - 115,000; Full time

Benefits offered by this job

401(k) plan

Medical, dental, vision insurance

Tuition reimbursement

Job summary

Bausch + Lomb is seeking a Sr. Clinical Trial role to support the planning, conduct, and closeout of clinical studies under the Director of Clinical Operations.

The position emphasizes GCP compliance, regulatory knowledge, and coordination with trial sites in the US and internationally. This role requires a Bachelor’s degree in a health field or science, 3+ years of clinical trials experience, excellent communication, and ability to work independently.

Qualifications

• Bachelor's degree in health profession or science; advanced degree a plus.
• At least 3 years of ongoing clinical trials experience.
• Proficiency in knowledge of GCPs and FDA regulatory requirements.
• Knowledge of medical terminology.
• Excellent verbal and written communication; able to work independently; computer proficiency (Word, Excel, Outlook).
• Travel may be required (minimal).

Responsibilities

• Collaborates with CTM/Sr. CTM on protocol development, CRF creation, IRB submissions, and site documentation.
• Supports regulatory compliance with FDA and international requirements.
• Coords communication with trial sites on conduct, monitoring, and study visits.
• Tracks study payments and invoices.
• Provides operational support to ensure efficient TMF and start-up activities.
• Teams with R&D, Regulatory, Safety, and Quality/Compliance groups.
• Assists with presentations of clinical information for projects.
• Handles moderate-to-high complexity tasks requiring judgment and flexibility.

Skills

GCP knowledge

FDA regulatory knowledge

Verbal communication

Written communication

Independent worker

MS Office

Education

Bachelor's degree in health profession or science

Advanced degree a plus

Tools

Word

Excel

Outlook

Job description

Bausch + Lomb is seeking a Sr. Clinical Trial role to support the planning, conduct, and closeout of clinical studies under the Director of Clinical Operations.

The position emphasizes GCP compliance, regulatory knowledge, and coordination with trial sites in the US and internationally. This role requires a Bachelor’s degree in a health field or science, 3+ years of clinical trials experience, excellent communication, and ability to work independently.