Clinical Research Manager, Neurology

This is a fully remote position, open to applicants in Maryland.

📋 Description

• Collaborate with investigators and utilize independent judgment to manage the research activities on behalf of the Principal Investigator (PI).

• Engage in scientific dialogues with collaborators, PIs, and funding agencies.

• Work alongside the PI to ensure the operational viability of the proposed protocol or study design.

• Create or supervise the creation of standard operating procedures and data collection forms derived from protocols.

• Formulate or oversee the creation of consent forms for clinical trials based on established protocols.

• Manage the preparation and submission processes for Institutional Review Board (IRB) and serve as the primary contact for regulatory compliance on behalf of the PI.

• Provide training and oversight for research data management and regulatory compliance.

• Collaborate with commercial and/or governmental sponsors to assess the appropriate group considering patient demographics, available resources, and service costs.

• Partner with the finance team to create study budgets, ensuring all costs associated with the study are included.

• Confirm that the clinical research protocol has a completed Prospective Reimbursement Analysis (PRA) and that processes and systems are established to follow the PRA when necessary.

• Maintain a robust system for tracking and reporting clinical research milestones for financial invoicing purposes.

• Monitor activities, systems, and processes to enhance referrals and boost enrollment in clinical trials.

• Ensure the development, testing, and assessment of manuals, questionnaires, and coding structures for efficient data collection.

• Oversee data collection at a single site or across multiple sites in a multi-centered clinical trial.

• Lead study meetings to review data, determine subsequent steps, implement operational changes to protocols based on outcomes and objectives, and initiate sub-studies.

• Contribute to the development of presentations and manuscripts.

• Recruit, supervise, and evaluate the performance of other exempt-level research staff.

• Perform additional duties as assigned.

⛳️ Requirements

• Bachelor's Degree in a relevant field.

• A minimum of five years of related experience in clinical research within an academic, government, or pharmaceutical industry setting.

• Proven experience in supervisory or leadership roles.

• Additional education may be accepted in lieu of the required experience, and extra related experience may replace the necessary education beyond a high school diploma or equivalent, as permitted by the JHU equivalency formula.

🏝️ Benefits

• Health insurance

• Retirement plans

• Paid time off

• Flexible work arrangements

• Professional development