Clinical Trial Manager - FSP at Parexel

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Key Accountabilities:

• Manage external vendors and contract research organizations
• Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual
• Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents
• Assist with protocol development and study report completion
• Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols
• Provide guidance, direction, and management to CRAs
• Track patient enrollment; qualify, initiate, monitor, perform closeout activities, and review site reports; and assist in coordination of data management activities
• Coordinate study supplies
• Negotiate contracts with vendors of clinical trial services
• Review Informed Consent Forms, CRFs, and study related materials
• Plan and participate in investigator meetings
• Assist and support data query process
• Ensures trial master file is current and maintained
• Collaborate in the management of external vendors and contract research organizations to ensure efficient execution of clinical trials.

Skills:

• Oversee all aspects of clinical trials from initiation to closeout, ensuring timely completion within budget through effective project management.
• Identify and resolve issues that arise in a timely manner during trial execution to minimize delays and maintain study integrity, employing strong problem-solving abilities.
• Effectively manage multiple tasks, deadlines, and priorities in a complex clinical trial environment
• Clearly convey information and expectations to cross-functional teams, investigators, and stakeholders

Knowledge and Experience:

• Good Clinical Practices (GCPs) and regulatory compliance (FDA and ICH guidelines)
• Experience in clinical trial documentation and processes (e.g., protocols, CRFs, monitoring plans)
• Experience of data management and query resolution in clinical trials
• Overall knowledge of site management and monitoring procedures

Education:

• Degree in the life sciences field preferred