Principal Investigator - Clinical Research

About Us:

ALSA Research is a leading clinical research network dedicated to advancing medical science and improving patient outcomes. We are are seeking a distinguished Principal Investigator with previous clinical research experience to join our dynamic team. We are willing to consider candidates from a variety of different medical specialities as long as they have previous clinical research experience as either a Principal Investigator or Sub-Investigator. Candidates must be licensed in the state of Connecticut and able to be physically present on-site for limited patient interactions (not expected to be there regularly).

Position Overview:

As a Principal Investigator, you will lead and oversee clinical research studies covering a range of therapeutic areas and indications. This role offers the unique opportunity to generate additional revenue by conducting clinical research, with full support provided to handle the administrative and operational aspects. This role is part-time based on the volume of studies we are working on and will require some in-person presence at our office in Bridgeport, Connecticut.

Opportunity Highlights:

• Flexible Schedule: Typical demand is 5-10 hours per week, per study. Study activities can often be completed in a single day, with additional scheduling options available.
• Compensation: Competitive compensation based on a percentage profit-sharing model from each clinical research study you participate in as a Principal Investigator.

Key Responsibilities:

• Implement research protocols for clinical trials across a variety of therapeutic areas. Lead the research team and ensure adherence to study protocols and ethical guidelines.
• Report adverse events in a timely manner; review sponsor provided safety reports.
• Review informed consent forms.
• Review the inclusion/exclusion criteria, endpoint criteria, and investigational article use with the internal research team.
• Provide medical support to Sub-Investigators and study staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
• Ensure compliance with all regulatory requirements, including IRB approvals, GCP guidelines, and federal and state regulations.
• Work closely with sponsors, CROs, and other research professionals to ensure successful study execution and maintain strong professional relationships.
• Supervise and mentor research staff, including sub-investigators, study coordinators, research nurses, and other team members involved in clinical trials.

Qualifications:

• Education: MD or DO license in good standing; board certification (we are willing to consider a variety of specialties)
• Experience: Minimum of 1 year of experience in clinical research. Proven track record of successfully overseeing and managing clinical trials.
• Skills: Strong knowledge of clinical research methodologies, regulatory requirements, and GCP. Excellent analytical, organizational, and communication skills.
• Personal Attributes: Detail-oriented, with the ability to work independently and as part of a collaborative team. Strong leadership skills and a commitment to advancing psychiatric research.

What We Offer:

• Competitive compensation
• Opportunity to generate additional revenue through clinical research
• Supportive and collaborative work environment
• Professional development and career growth opportunities
• Ability to work remotely or from your own private practice

Application Process:

Interested candidates should submit a resume/CV, preferably a cover letter detailing relevant experience and research interests, and contact information for professional references.

ALSA research is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Work Location: In person (Bridgeport, Connecticut)