Associate Director, Global Study Operations, Program Lead

Proclinical Group; San Francisco (CA); Remote; USD 120,000 - 180,000; Full time

Job summary

Proclinical is looking for an Associate Director for Global Study Operations, focusing on rare diseases, to oversee program execution and foster collaboration in clinical trials. The role involves strategic planning, effective communication, and leading change management initiatives within a matrix organization.

Qualifications

• Significant experience in clinical trials or drug development.
• Experience in team management.
• Strong background in study design and vendor management.

Responsibilities

• Overseeing program execution and cross-functional collaboration.
• Driving innovation in clinical trial processes.
• Acting as the primary point of escalation for program execution issues.
• Mentoring and managing team members.

Skills

Communication

Leadership

Decision-making

Data analytics

Clinical trial delivery

Education

BA/BS degree in life sciences or related field

Advanced degree preferred

Job description

Associate Director - Permanent - Remote (CA)

Are you a dedicated individual looking to put your expertise to work fully flexibly in a remote position?

Proclinical is seeking an Associate Director for Global Study Operations to lead and manage clinical programs with a focus on rare diseases.

Primary Responsibilities:

The successful candidate will be involved in overseeing program execution, fostering cross-functional collaboration, and driving innovation in clinical trial processes. You will be instrumental in ensuring successful outcomes through strategic planning and effective communication.

Skills & Requirements:

• Strong communication, leadership, and decision-making skills.
• Experience in drug development, study design, and vendor management.
• Proficiency in data analytics and interpretation.
• Advanced knowledge in clinical trial delivery and recruitment practices.
• BA/BS degree in life sciences or related field; advanced degree preferred.
• Significant experience in clinical trials or drug development, with team management experience.

The Associate Director's responsibilities will be:

• Contribute to the clinical development strategy and operationalize the Clinical Development Plan.
• Provide program-level oversight, ensuring deliverables are met within timelines and budget.
• Act as the primary point of escalation for program and study execution issues.
• Drive and implement cross-functional initiatives to enhance clinical program efficiency.
• Champion change management and support staff through transitions.
• Mentor and manage team members within a matrix organization.

If you are having difficulty in applying or if you have any questions, please contact Nico Kohlwes at [e-mail]

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy