Senior Clinical Trial Manager - Spain - FSP

About this role

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. External Job Description At Parexel people make the difference. We have a crucial mission: to prevent and cure disease by delivering important new medicines and therapies to patients in need. We achieve this important goal through the knowledge, expertise, innovation, and commitment of our employees around the world. Our employees have the opportunity to do meaningful things globally while we support them locally in environments full of challenge, collaboration, flexibility and industry-leading growth potential.

Parexel FSP is recruiting for a Clinical Trial Manager based in Spain . Home based role. Dedicated to a single sponsor. You will will manage individual oncology clinical trials and/or programs as part of the Clinical Trial Working Group. Tasks on the role 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 Jazz Pharmaceuticals’ SOPs and FDA and ICH guidelines 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.