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Neuroscience Clinical Research Specialist
2 months ago
Our mission is to redefine the landscape of clinical research.
With extensive expertise and a team of exceptional professionals, we assist the global biopharmaceutical sector in expediting the introduction of innovative medical therapies to the market.
We aspire to make a significant impact on the world, and with the collaboration of our teams worldwide, we thrive collectively. At Calyx, we operate as one cohesive unit. We learn, develop, and succeed together.Are you prepared to contribute to transformative change?
In addition to fulfilling work, we offer:
HEALTH:
- Comprehensive Medical, Dental, and Vision coverage for you and your family, including Flexible Spending Accounts (FSA) and Health Savings Accounts (HSAs)
PERSONAL DEVELOPMENT:
- Generous paid time off policy encompassing holidays and sick leave
- Opportunities for internal growth and professional development programs
FINANCIAL SECURITY:
401(k) plan, life and accident insurance, and disability coverage.
Role Overview
This is a remarkable opportunity to engage at the forefront of clinical drug development as we strive to accelerate the delivery of pioneering therapies aimed at enhancing patient outcomes.
We are a well-respected and expanding clinical research and medical imaging organization with significant initiatives in both pre-clinical and clinical domains.
This position is ideally suited for a board-certified or board-eligible Neurologist or Psychiatrist with a keen interest in clinical trials.
We are looking for a physician to become part of our ongoing clinical research program.
Our facility is dedicated to research (with no fees or insurance required), where we conduct globally recognized studies in Parkinson's Disease, Alzheimer's Disease, and other neurological disorders.
The clinical team consists of physicians, advanced practice providers, nurses, nuclear medicine technologists, and coordinators. The successful candidate will take on the role of principal investigator or sub-investigator for both single-site and multi-site studies.
This position entails overseeing study execution, ensuring participant safety, and collaborating with interdisciplinary teams (including Project Management, Chemistry, Regulatory Affairs, Quality Assurance, Image Analysis, Data Management, Medical Writing, etc.) to meet project objectives.
Key Responsibilities
Assume the role and responsibilities of principal investigator/sub-investigator/site physician and provide comprehensive supervision and management of studies within the facility.
The investigator will conduct and coordinate daily clinical trial activities in accordance with ICH/FDA/GCP guidelines, local regulations, study protocols, and company policies.
Provide medical and clinical oversight for all activities conducted within the facility.
Ensure appropriate delegation of responsibilities to qualified staff.
Maintain high-quality standards for clinical work and outcomes.
Engage with local neurologists, physicians, community outreach organizations, and international medical/scientific experts.
Identify eligible participants and manage recruitment for multiple concurrent studies.
Educate potential or enrolled participants regarding trial opportunities.
Collect, compile, and document patient medical information, including health histories, progress notes, and results from physical examinations.
Conduct or supervise structured evaluations and procedures in clinical trials. Monitor participants for adverse events and initiate appropriate actions based on clinical judgment.
Review and assess safety data; evaluate and report safety incidents, protocol deviations, and other protocol-specific documentation.
Provide clinical and scientific leadership within the organization and contribute to clinical strategy and plans aligned with business unit and company priorities.
Collaborate with operational and management teams to ensure departmental objectives are achieved.
Other responsibilities as required.
Qualifications:
MD or DO degree with a valid medical license.
Must possess, or be able to obtain, an active medical license.
Eligibility to serve as Principal Investigator for Clinical Trials in the US.
Demonstrate the necessary education, training, and experience to conduct clinical investigations.
Advanced understanding of treatment protocols and drug interactions.
Ability to establish rapport with participants, neurologists, and biopharmaceutical sponsors.
Strong interpersonal skills for effective collaboration with participants and multidisciplinary management teams.
Proficient in electronic communication methods (e.g., Email, Video Conferencing, Slack, etc.).
Computer literacy, including strong knowledge of software applications and proficiency in Microsoft Office, with the ability to learn new software.
Preferred Qualifications:
Specialty training and board certification/eligibility in Neurology or Psychiatry.
Sub-specialty training in CNS disorders is advantageous.
Experience as a principal investigator or sub-investigator in clinical studies.
Experience in conducting clinical pharmacology studies.
Familiarity with clinical research methodologies, including recent advancements in biomarkers, efficacy measures, diagnostic practices, study designs, safety evaluations, and regulatory standards.
Knowledge of molecular imaging principles.
Experience in a clinical research organization and/or a minimum of 5 years in a scientific, research, or healthcare setting.
Experience with patients suffering from CNS disorders (e.g., Neurodegenerative disorders, Movement disorders, Psychiatric disorders, Multiple Sclerosis, etc.) or oncology.
Other Information
This position follows a standard Monday to Friday schedule: 8am-5pm. It may require alternative or additional hours, including weekends or evenings, to ensure adequate study coverage. This position is based at our dedicated research facility and does not offer hybrid or remote work options.
Occupational Exposure/Risk Potential:
- Bloodborne pathogens or bodily fluids (Applicable)
- Ionizing Radiation Exposure (Applicable)
We are proud to be an Equal Employment Opportunity employer.
We do not discriminate based on race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, veteran status, disability, or any other legally protected characteristics.
