Clinical Research Coordinator

Seeking an experienced, motivated Clinical Research Coordinator looking to grow into a full time role for a busy retina practice. We are also willing to train a current Ophthalmic Technician into this position, if needed. This position provides an excellent opportunity for career advancement as well as personal growth and development. Superior organization and time management skills are mandatory. This is a highly autonomous position for a self-reliant individual that is dependable, yet able to work well in a team environment. We are looking to hire immediately. Must be a resident of Indiana as this is an in-office position and must be legally authorized to work in the United States.

The right candidate will be responsible for:

• All regulatory demands for assigned studies.
• The oversight of day to day study requirements.
• Scheduling study subjects for assigned studies.
• Preparing and conducting subject visits.
• Organization of all documents to the department’s standards.
• Technical skills that include visual acuity and refraction (loose lens), applanation IOP, slit lamp exams, OCT. Able and willing to learn to perform ECGs, blood draws, lab sample preparation and shipment.
• Computer data entry.
• Attending mandatory meetings.
• Maintain department mandatory training and certifications.

Position includes:

• Competitive pay depending on experience and certifications
• Flexible hours
• Benefit package
• Occasional travel

KNOWLEDGE, SKILL and ABILITIES REQUIRED:

• Ability to observe, assess, and record symptoms, reactions, and progress.
• Skill in the use of computerized systems and databases.
• Ability to communicate effectively, both orally and in writing.
• Knowledge of the principles and procedures of clinical research.
• Knowledge of accreditation and certification requirements and standards.
• Ability to maintain quality, safety, and/or infection control standards.
• Ability to provide direct patient care and consultation to patients.
• Records maintenance skills.
• Ability to maintain confidentiality of records and information.
• Strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in a diverse community.
• Knowledge of inventory management practices.
• Skill in organizing resources and establishing priorities.
• Ability to recruit, evaluate and instruct clinical research subjects and volunteers.
• Ability to prepare and process laboratory samples using established protocols.
• Knowledge of FDA regulations.
• Knowledge of relevant policies, procedures, and regulations pertaining to the release of confidential information.
• Ability to understand and follow specific instructions and procedures.

MINIMUM JOB REQUIREMENTS:

Preferred JCAHPO Certified Ophthalmic Assistant, Technician or Technologist (must maintain certification) with the ability to display the knowledge, skills and abilities as required.

Preferred Certified Clinical Research Coordinator – Or working towards this level of certification.

Job Type: Full-time

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible schedule
• Flexible spending account
• Health insurance
• Life insurance
• Paid time off
• Retirement plan
• Tuition reimbursement
• Vision insurance

Work Location: In person