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Sponsor Dedicated Global Project Manager Ii - Home Based In Spain

10 Dec. 2, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Sponsor Dedicated Global Project Manager II

Updated: November 22, 2024
Location: Spain (Home-Based, Madrid)
Job ID: 24006371


Role Overview

Syneos Health is hiring a Sponsor Dedicated Global Project Manager II based in Spain. This role requires robust expertise in global study and project management, ideally in Phase I or Phase IV clinical trials, with a focus on operational leadership and sponsor relations.


Core Responsibilities

Project Leadership and Coordination

  • Serve as the primary contact between Syneos Health and the sponsor, ensuring seamless execution of studies.

  • Oversee global clinical research studies from initiation to closeout, adhering to Good Clinical Practice (GCP), company SOPs, and regulatory requirements.

  • Lead cross-functional teams to achieve study objectives within established timelines and budgets.

  • Address project challenges proactively, implementing risk mitigation strategies.

Operational and Quality Oversight

  • Ensure all trial documentation is complete and compliant for audit readiness, including Trial Master Files (TMF).

  • Develop and execute detailed project plans and monitor study deliverables using appropriate systems.

  • Facilitate and present in internal and sponsor meetings, providing clear project updates.

Stakeholder and Business Relations

  • Cultivate and maintain sponsor relationships, identifying potential opportunities for new or extended collaborations.

  • Represent Syneos Health in bid defense meetings when proposed as the project lead.

Management and Development

  • Supervise and mentor other project management and clinical operations staff when required.

  • Foster collaboration across teams and provide guidance on project best practices.


Candidate Profile

Essential Qualifications

  • Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or an equivalent field.

  • Proven experience in global study management and clinical project management.

  • Familiarity with CRO operations and relevant therapeutic areas.

Preferred Experience

  • Direct involvement in Phase I and/or Phase IV clinical trials.

Key Skills

  • Strong knowledge of GCP/ICH guidelines and regulatory requirements.

  • Exceptional organizational and time-management abilities.

  • Proficiency in embracing and implementing new technologies.

  • Excellent written and verbal communication, presentation, and interpersonal skills.

  • Willingness to travel up to 25% of the time.


Why Syneos Health?

Global Impact

  • Work on groundbreaking projects contributing to 94% of FDA-approved novel drugs and 95% of EMA-authorized products over the last five years.

Career Growth and Support

  • Access to career development programs, peer recognition, and training opportunities.

  • A supportive environment emphasizing inclusion, diversity, and the Total Self culture, where employees are encouraged to be authentic and innovative.


Application Information

Seize the opportunity to advance your career and make a difference in global healthcare. Apply now or join the Talent Network to explore more opportunities with Syneos Health.