Clinical Trial Manager - FSP

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.

Job Overview

​​The Clinical Trials Manager (CTM) will be a member of client’s Development Operations team. The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group.​​

Key Accountabilities :

Oversight of activities

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

Assure regulatory compliance of investigational sites with client’s SOPs and FDA and ICH guidelines

Ensures trial master file is current and maintained

Collaborative relationships

Collaborate in the management of external vendors and contract research organizations to ensure efficient execution of clinical trials.

Compliance with Parexel standards

Complies with required training curriculum

Completes timesheets accurately as required

Submits expense reports as required

Updates CV as required

Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements

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