Careers

Position Overview
We are seeking a motivated Clinical Research Coordinator (CRC) to join our physician-led clinical research team. This role is designed as a structured training and advancement pathway, beginning with participant recruitment and progressing to full CRC responsibilities on both internal and industry-sponsored clinical trials.

Role Progression & Responsibilities
• Participant Recruitment & Pre-Screening
Learn to identify, engage, and evaluate treatment-seeking potential research participants
Conduct initial eligibility assessments and support informed consent workflows
Build strong communication skills with participants and their families
• Administrative & Study Operations Training
Learn the administrative foundations of clinical research, including documentation, scheduling, and protocol adherence
Integrate operational responsibilities alongside recruitment activities
• Transition to CRC Responsibilities
Gradually transition from recruitment-focused work to coordinating internal, self-sponsored clinical trials
Advance to industry-sponsored trials after demonstrating competency, reliability, and attention to detail
• Clinical & Procedural Training
• Receive hands-on training in medical and research procedures, with increasing complexity based on comfort and proficiency
• Opportunities to learn and safely perform:
Phlebotomy
Electrocardiograms (ECGs)
Additional study-specific clinical procedures
• Exposure to diagnostic and assessment tools, including opportunities to train in FibroScan and basic independent neuropsychiatric interviewing
• Professional Development & Education
Formal training in Good Clinical Practice (GCP) and clinical research operations
Ongoing mentorship through small-group training sessions led by physicians
Development of collaborative skills within a multidisciplinary, multispecialty research team

Why This Role
This position is ideal for individuals seeking hands-on entry into clinical research with clear growth opportunities, close physician mentorship, and exposure to high-quality trial conduct.

To apply, please send your CV and cover letter to careers@basilclinical.com.

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About Basil Clinical

At Basil Clinical, we partner with leading pharmaceutical and biotech companies to conduct trials across Neurology, Psychiatry, Internal Medicine, and Oncology. Our principal investigators are deeply committed to both scientific advancement and participant care— ensuring that every study is conducted with rigor, transparency, and compassion.

Through advanced recruitment strategies, real-time eSource documentation, and centralized quality oversight, we streamline trial execution while safeguarding data integrity. By combining deep clinical expertise with cutting-edge infrastructure, Basil Clinical consistently delivers reliable data and meaningful outcomes.

We believe better data begins with better access. That’s why we focus on providing equal opportunity for participation to diverse, underrepresented populations— while maintaining the highest standards of Good Clinical Practice.

Company Description
Basil Clinical is a physician-led research organization that accelerates clinical trials through operational excellence, high-volume inclusive recruitment, and data-driven precision. We partner with leading pharmaceutical and biotech companies to conduct trials in Neurology, Psychiatry, Internal Medicine, and Oncology. Our principal investigators are committed to both scientific advancement and participant care, ensuring rigorous, transparent, and compassionate studies. By focusing on diverse and underrepresented populations, we maintain the highest standards of Good Clinical Practice and deliver reliable data and meaningful outcomes through advanced recruitment strategies and centralized quality oversight.

Role Description
This is a full-time on-site role for a physician located in Queens, New York. The Clinical physician will be responsible for overseeing trials, providing care, working collaboratively with a multidisciplinary team, and maintaining comprehensive documentation. They will provide specialized care and contribute to scientific research through rigorous and compassionate patient care.

Responsibilities

• Lead study team as Sub-Investigator and eventually Principal, ensuring trials are conducted safely and per protocol
  Conduct clinical intake interviews to determine medical eligibility of potential study participants
• Educate potential participants about diseases and the benefits of clinical trial participation
• Manage the safety of study participants; respond appropriately to adverse events in a timely manner
• Provide medical leadership to our team and study coordinators

Requirements

• Valid license to practice medicine in New York
• Board-certified/eligible in psychiatry
  Experience working with older adults in a clinical or research setting
• Clinical research experience is preferred, but not required
• A command of professional spoken and written English

To apply, please send your CV and cover letter to careers@basilclinical.com.

-------------------------------------------------------------------------------------------------------------------------------

About Basil Clinical

At Basil Clinical, we partner with leading pharmaceutical and biotech companies to conduct trials across Neurology, Psychiatry, Internal Medicine, and Oncology. Our principal investigators are deeply committed to both scientific advancement and participant care— ensuring that every study is conducted with rigor, transparency, and compassion.

Through advanced recruitment strategies, real-time eSource documentation, and centralized quality oversight, we streamline trial execution while safeguarding data integrity. By combining deep clinical expertise with cutting-edge infrastructure, Basil Clinical consistently delivers reliable data and meaningful outcomes.

We believe better data begins with better access. That’s why we focus on providing equal opportunity for participation to diverse, underrepresented populations— while maintaining the highest standards of Good Clinical Practice.

Company Description
Basil Clinical is a physician-led research organization that accelerates clinical trials through operational excellence, high-volume inclusive recruitment, and data-driven precision. We partner with leading pharmaceutical and biotech companies to conduct trials in Neurology, Psychiatry, Internal Medicine, and Oncology. Our principal investigators are committed to both scientific advancement and participant care, ensuring rigorous, transparent, and compassionate studies. By focusing on diverse and underrepresented populations, we maintain the highest standards of Good Clinical Practice and deliver reliable data and meaningful outcomes through advanced recruitment strategies and centralized quality oversight.

Role Description
This is a full-time on-site role for a Neuropsychologist located in Queens, New York. The neuropsychologist will be responsible for administering cognitive assessments, working collaboratively with a multidisciplinary team, and maintaining comprehensive documentation. The ideal candidate will have experience administering structured and semi-structured cognitive assessments, including ADAS-Cog, MMSE, MoCa, MADRS, and other standardized scales used in clinical trials.

Responsibilities:

• Conduct neuropsychological assessments per protocol
• Administer and score structured/semi-structured interviews (e.g., SCID, CDR)
• Ensure adherence to GCP and sponsor training requirements
• Maintain accurate source documentation and data integrity

Requirements:

• PhD or PsyD in Psychology, Neuropsychology, or related field
• Clinical trials experience with CNS/Alzheimer’s preferred
• Certification on rating scales a plus
• Strong communication and documentation skills

To apply, please send your CV and cover letter to careers@basilclinical.com.

-------------------------------------------------------------------------------------------------------------------------------

About Basil Clinical

At Basil Clinical, we partner with leading pharmaceutical and biotech companies to conduct trials across Neurology, Psychiatry, Internal Medicine, and Oncology. Our principal investigators are deeply committed to both scientific advancement and participant care— ensuring that every study is conducted with rigor, transparency, and compassion.

Through advanced recruitment strategies, real-time eSource documentation, and centralized quality oversight, we streamline trial execution while safeguarding data integrity. By combining deep clinical expertise with cutting-edge infrastructure, Basil Clinical consistently delivers reliable data and meaningful outcomes.

We believe better data begins with better access. That’s why we focus on providing equal opportunity for participation to diverse, underrepresented populations— while maintaining the highest standards of Good Clinical Practice.