Senior Director of Clinical Research

Overview:

The Senior Clinical Research Manager will lead and direct clinical trials and research studies, ensuring timely completion, compliance with regulatory standards, and optimal results.

Key Responsibilities:

• Clinical Trial Leadership:

  1. Develop, implement, and manage clinical research projects from initiation to completion.
  2. Coordinate and oversee the execution of clinical trials, adhering to protocols, timelines, and quality standards.
  3. Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and ethical guidelines.
  4. Provide oversight on the recruitment, enrolment, and monitoring of clinical trial subjects.
  5. Manage relationships with clinical research organizations (CROs), investigators, and external partners.

• Team Management:

  1. Lead, mentor, and develop clinical research staff, ensuring they are trained and performing effectively.
  2. Assign tasks and responsibilities to team members based on project needs.
  3. Develop training programs and provide ongoing professional development for research teams.

• Regulatory Compliance:

  1. Oversee the preparation and submission of regulatory documentation, including Institutional Review Board (IRB) applications and clinical trial applications.
  2. Monitor compliance with federal, state, and local regulations, as well as company policies.
  3. Ensure timely reporting of adverse events and adherence to study protocols.

• Study Design & Protocol Development:

  1. Collaborate with scientific and medical teams to develop clinical trial protocols.
  2. Ensure protocols meet study objectives, regulatory standards, and ethical guidelines.
  3. Evaluate feasibility and risk of proposed studies.

• Data Management and Reporting:

  1. Ensure data collection, monitoring, and analysis are conducted efficiently and accurately.
  2. Review and analyze clinical trial data to ensure quality and integrity.
  3. Prepare and present progress reports to senior leadership and stakeholders.

• Budget and Resource Management:

  1. Develop and manage project budgets, ensuring timely completion within financial constraints.
  2. Oversee resource allocation, including personnel, equipment, and materials.

• Collaboration and Communication:

  1. Foster communication between internal teams, external partners, and key stakeholders.
  2. Collaborate with clinical research coordinators, data managers, and other departments to ensure effective study execution.
  3. Resolve any issues related to clinical trial execution and provide solutions.

• Continuous Improvement:

  1. Identify areas for process improvement in clinical trial execution and management.
  2. Implement best practices to optimize research efficiency and compliance.

Qualifications and Skills:

• Education:

  1. Bachelor's degree in Life Sciences, Clinical Research, or a related field (Master's or higher preferred).

• Experience:

  1. 8 to 18 years of experience in clinical research, with at least 2-3 years in a managerial or supervisory role.
  2. In-depth knowledge of clinical trial management, regulatory requirements, and GCP.

• Skills:

  1. Strong project management, leadership, and organizational skills.
  2. Excellent communication and interpersonal skills, with the ability to interact effectively with internal and external stakeholders.
  3. Proficiency in clinical research software and data management systems.
  4. Strong problem-solving and decision-making abilities.

Responsibilities Include:

• Development and implementation of clinical research projects

• Leadership and management of clinical research teams

• Collaboration with cross-functional teams to ensure effective study execution

• Development and maintenance of strong working relationships with CROs, investigators, and external partners

About This Role:

This is an exciting opportunity for a highly motivated and experienced Senior Clinical Research Manager to join our team. If you have a passion for clinical research and excellent leadership and management skills, we encourage you to apply.