Ophthalmology/Optometry Consultant – Clinical Research at Adams Clinical
Watertown, MA 02472, USA -
Full Time


Start Date

Immediate

Expiry Date

08 Nov, 25

Salary

500.0

Posted On

09 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Communication Skills

Industry

Hospital/Health Care

Description

Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions.
We are seeking a licensed and experienced Ophthalmologist or Optometrist to serve as a part-time consultant for clinical research studies. This role involves performing comprehensive eye examinations, documenting findings according to study protocols, and supporting the study team with ophthalmic expertise. Ideal for professionals seeking flexible, as-needed work with no fixed schedule. The Adams Clinical Site Network has locations in Watertown, MA; Boston, MA; Harlem, NY; Bronx, NY; Philadelphia, PA; and Dallas, TX.

QUALIFICATIONS:

  • Licensed and in good standing to practice as an Ophthalmologist (MD/DO) or Optometrist (OD) in Massachusetts
  • Detail-oriented with good documentation and communication skills
  • Flexible availability to work on an as-needed basis with variable scheduling
  • Prior training in the administration of therapy within industry-sponsored psychedelic trials (e.g., Compass, Cybin, MindMed, Atai) is a significant plus
  • This role is well suited for individuals with a strong interest in psychedelic research and its clinical applications, especially those looking to contribute meaningfully to the development and refinement of therapeutic protocols in this emerging field.
Responsibilities

Perform full, protocol-specified ophthalmic or optometric examinations on research participants, including:

  • Visual acuity testing
  • Refraction (manifest and/or cycloplegic as needed)
  • Intraocular pressure measurement
  • Slit lamp biomicroscopy
  • Indirect ophthalmoscopy
  • Gonioscopy

Interact with participants, perform examinations and document all findings in accordance with Good Clinical Practice (GCP)
Maintain accurate and secure clinical records
Communicate findings to the principal investigator and study team as needed
Comply with all applicable regulatory and institutional guidelines
Participate in training on protocol-specific requirements (as needed)

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