Mental Health Professional

About the role

Adams Clinical invites you to join a mission-driven team dedicated to accelerating the development of life-changing medicines through uncompromising data quality and safety. In this role, you will own the delivery of high-quality psychiatric and neurological assessments within a collaborative, multicultural trial environment that values scientific rigor and authentic collaboration. You will be responsible for ensuring that all participant interactions reflect the highest standards of integrity, transparency, and continuous improvement. This position places you at the forefront of clinical innovation, where your expertise will directly influence the success of late-phase trials and the lives of participants. You will partner closely with sponsors and cross-functional teams to uphold the gold standard for clinical trial excellence. Together, we will create an environment where meaningful work drives meaningful change and where professional growth is actively supported. If you are passionate about making an impact and want to contribute to groundbreaking research, this is your opportunity to join a team committed to diversity, equity, and inclusion.

Key facts

What you'll do

Conduct screening interviews and diagnostic evaluations to determine participant eligibility for clinical trials and coordinate appropriate follow-up actions.

Administer psychiatric and neuropsychological rating scales and assessments to ensure accurate and reliable data collection for study protocols.

Perform differential diagnoses and comprehensive clinical evaluations to support trial eligibility and participant safety.

Gather and document detailed clinical histories, including substance use patterns, to inform trial suitability and risk assessment.

Collaborate with study leadership to align assessment schedules and procedures with protocol timelines and regulatory requirements.

Support the implementation of training procedures to maintain consistency in assessment administration across the clinical team.

Monitor participant progress and report any adverse events or deviations to ensure compliance with ethical and regulatory standards.

Engage in continuous learning by attending workshops, seminars, and internal training sessions to refine clinical and procedural skills.

Contribute to the improvement of trial methodologies by providing feedback based on participant interactions and clinical observations.

Foster an atmosphere of authentic collaboration by working respectfully with diverse teams, sponsors, and study personnel.

Ensure that all documentation is completed accurately, thoroughly, and in a timely manner to support data integrity and audit readiness.

Promote a culture of respect and transparency by communicating clearly with participants, families, and healthcare providers.

Support recruitment and retention efforts by building trust and rapport with potential trial candidates and their communities.

Demonstrate commitment to operational excellence by adhering to standard operating procedures and quality assurance guidelines.

Requirements

Hold a PhD or PsyD in Clinical or Counseling Psychology from an accredited institution.

Possess a valid LCSW, LMSW, LMHC, or equivalent New York State mental health licensure.

Candidates with a master's degree in a mental health-related field may also qualify if degree limitations are met.

Degrees in art therapy, expressive therapies, or non-clinical master's programs will not meet the requirements for this role.

Bring a minimum of 2 years of direct clinical experience, including diagnostic evaluations, administering assessments, and delivering patient care in psychiatry or related healthcare settings.

Demonstrate strong experience in conducting differential diagnoses, as this skill is essential for accurate participant screening.

Prior experience with substance use disorders will be viewed as a significant advantage in this position.

Exposure to clinical trials or neuropsychological assessments is preferred, as structured training will be provided to bridge any gaps.

This role is not suitable for recent graduates lacking clinical experience or for clinicians seeking positions that focus primarily on direct therapy services.

Must be authorized to work in the United States and not require sponsorship for the position at this time.

Commit to working full-time on-site during standard business hours, with occasional evening hours as study needs require.

Nice to have

Previous exposure to late-phase psychiatry and neurology clinical trials.

Experience working with diverse populations and multicultural trial participants.

Familiarity with electronic data capture systems and clinical trial software.

Knowledge of current regulations and guidelines governing clinical research.

Skills in advanced statistical analysis or research methodology.

Practical notes

This is a full-time, on-site role based in Bronx, New York, with typical business hours and occasional evening requirements. No travel, visa, or specific deadline information is provided in this listing.