Summary
The Clinical Research Investigator will lead clinical research activities with a strong commitment to participant safety and regulatory compliance. This role includes overseeing clinical assessments, interpreting study protocols, collaborating with key stakeholders, and ensuring ethical conduct throughout all phases of the study. The investigator will play a crucial role in participant recruitment strategies, protocol development, and maintaining the highest standards of medical and clinical practice.
Responsibilities
Lead and oversee clinical research activities to ensure compliance with regulatory requirements and ethical standards.
Ensure the well-being and safety of participants through safe study execution.
Interpret protocols and Investigator Brochures (IB) and strategize for patient recruitment initiatives.
Conduct clinical evaluations and assessments to confirm participant eligibility for studies.
Protect participant welfare and safety by adhering to ethical conduct.
Fulfill all medical duties as outlined by protocol, SOP/COP, ICH GCP, and local regulations.
Exercise meticulous attention to detail in documentation and patient care.
Collaborate with internal and external stakeholders, including regulatory authorities and sponsors.
Actively participate in protocol development, investigator meetings, and other research-related activities.
Requirements
Qualifications:
Valid medical degree (MD, DO, or equivalent).
Active medical license in the state of Maryland, in good standing, with unrestricted ability to practice as required.
Proficiency in general medical diagnosis and treatment.
Reliable commute or intent to relocate before starting work.
Prior experience as a clinical research investigator (principal or sub-investigator) is preferred.
Board certification or eligibility in Genetics, Biochemical Genetics, Acute Care, Intensive Care, or Neurology is preferred.
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