Clinical Research Coordinator II

Bausch + Lomb is a global eye health company dedicated to protecting and enhancing sight through its portfolio of eye health products. The Clinical Research Coordinator II independently coordinates and oversees clinical studies of moderate complexity, ensuring study objectives, timelines, documentation, and regulatory requirements are met. The role also leads study start-up and close-out activities, resolves operational issues, and mentors research personnel.

Responsibilities

Manages, coordinates, and implements clinical studies of moderate complexity independently

Serves as primary coordinator on assigned studies

Anticipates and resolves study operational issues, escalating when appropriate

Mentors and trains CRC I staff and other personnel

Leads study start-up, monitoring visit preparation, and close-out activities

Identifies opportunities for process improvement and operational efficiencies

Maintains study documentation according to standard operating procedures

Carries out study duties from protocol initiation to study close-out

Adheres to regulatory guidelines and standard operating procedures

Works closely with study team members

Uses existing procedures to solve routine or new problems

Completes study-related and other administrative tasks

Complies with Good Clinical Practice and the Code of Federal Regulations

Keeps current with all federal, state, sponsor and site policies and laws, standard operating procedures, and guidelines

Demonstrates accountability for learning in accordance with GCP guidelines

Keeps current with industry standards, best practices and trends in areas relevant to research studies and designs

Preferred

Candidates with a bachelor's degree in a scientific, health related, or business administration program, preferred

contact lens knowledge is preferred

Bachelor’s degree in science

business administration

Contact lens knowledge

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

U.S. based employees may be eligible for short-term and/or long-term incentives

U.S. based employees may be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others

U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation

Company

Global supplier of eye health products and surgical devices

Bridgewater, NJ, US

http://www.bausch.com/

Founded in 1853

10001+ employees

Qualifications

At minimum, candidates should have an associate's degree and/or related industry experience

Be detail-oriented, organized and manage time effectively

Demonstrate strong follow-through skills and flexibility

Possess the ability to identify and (proactively) solve problems

Demonstrate a professional demeanor

Possess excellent interpersonal skills

Possess exceptional written and verbal communication skills

Possess the ability to multi-task and manage deadlines

Possess the ability to work well independently as well as in team environment

Be proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook, Teams, SharePoint) and databases used in research environment or have a willingness to learn and demonstrate proficiency within six months of hire

Be knowledgeable of GCP, federal, state, and local regulations, policies and procedures or willing to learn within six months of hire

Have at least 3-5 years of experience in a clinical research environment

Demonstrated ability to independently coordinate studies

Ability to manage multiple studies simultaneously

Experience training or mentoring research personnel

Advanced knowledge of GCP and applicable regulatory requirements

Have basic medical and scientific knowledge

Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time

Candidates with a bachelor's degree in a scientific, health related, or business administration program, preferred

Contact lens knowledge is preferred

Have at least 3-5 years of experience in a clinical research environment.

Required skills

Clinical Research, Clinical Study Coordination, Clinical Practice (GCP), Clinical Research Regulations, Microsoft Office, Research Databases, Medical and Scientific Knowledge, Contact Lens Knowledge

Preferred skills

contact lens knowledge is preferred

Experience

3-5 years