Clinical Research Patient Engagement Specialist - Psychiatry

The role involves conducting patient screening and engagement for psychiatric clinical trials, focusing on Major Depressive Disorder, ensuring compliance with regulations, and collaborating with healthcare professionals to facilitate research.

Location: Remote (US)

Responsibilities

• Promote the mission of Javara with a focus on patient safety and well-being.
• Ensure safety, regulatory compliance, and adherence to SOPs and guidelines.
• Oversee application of patient engagement technology systems, policies, and procedures.
• Conduct telephone and in-person prescreening of prospective participants for psychiatric trials, primarily MDD.
• Build trust and rapport with individuals experiencing depression and other mental health conditions.
• Assess eligibility using protocol-specific criteria and document outcomes.
• Identify and escalate safety concerns, including suicidal ideation or psychiatric deterioration.
• Collaborate with investigators, coordinators, therapists, and referral sources to facilitate enrollment.
• Maintain a compassionate, patient-centered experience while meeting enrollment goals.

Requirements

• Bachelor’s degree in psychology, social work, counseling, nursing, or related healthcare field preferred (or equivalent relevant experience).
• Minimum of 2 years of professional experience working directly with adults diagnosed with Major Depressive Disorder or other serious mental health conditions.
• Experience in outpatient behavioral health, psychiatric practice, community mental health, inpatient psychiatry, crisis services, or clinical research involving psychiatric populations.
• Ability to communicate with patients experiencing depression, anxiety, or other psychiatric symptoms with empathy and professionalism.
• Experience conducting structured interviews, patient assessments, or clinical screening.
• Strong documentation and organizational skills with attention to detail.
• Comfortable working toward recruitment and enrollment goals in a fast-paced environment.
• Ability to adhere to SOPs, GCP guidelines, and regulations pertaining to clinical trials.
• Ability to take initiative, problem solve, and work independently.
• Accountable, dependable, and committed to quality work.
• Strong written and verbal communication skills.