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Global Clinical Project Manager Ii. Spain. Sponsor Dedicated

0-1 years
Not Disclosed
10 Nov. 29, 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

Project Manager II

Company: Syneos Health
Location: Flexible (Remote/On-site depending on the position)


About Syneos Health

Syneos Health is a global leader in biopharmaceutical solutions, designed to accelerate customer success by translating clinical, medical, and commercial insights into impactful outcomes. The organization focuses on simplifying and streamlining the clinical development process, aiming to put the customer and patient at the heart of everything.

With a workforce of 29,000 employees in 110 countries, Syneos Health drives innovation to deliver therapies faster, ultimately aiming to change lives.


Why Syneos Health?

  • Career Growth: Passionate about developing its people, Syneos Health offers opportunities for career progression through training, mentorship, and technical development.

  • Inclusive Culture: Syneos Health promotes a Total Self culture, where employees are encouraged to bring their whole selves to work, fostering a diverse and inclusive environment.

  • Global Impact: Join a company that works on cutting-edge therapies, having been involved in 94% of all FDA novel drug approvals in the past 5 years.


Role Overview

As a Project Manager II, you will oversee interdisciplinary clinical research studies, ensuring compliance with Good Clinical Practices (GCP) and regulatory requirements. This position will manage project teams to ensure the timely, quality-driven, and financially successful delivery of clinical trials. You will also be the primary liaison between the company and the customer, handling everything from study initiation to closeout.


Key Responsibilities

Project Leadership and Delivery

  • Manage Projects: Oversee the planning and execution of clinical studies, ensuring adherence to protocols, timelines, and budgets.

  • Team Leadership: Lead cross-functional project teams, driving study milestones and ensuring all deliverables are met.

  • Compliance Oversight: Ensure studies comply with GCP, SOPs, and regulatory requirements.

  • Financial Accountability: Manage the financial aspects of each project, ensuring the project remains within budget.

Documentation and Reporting

  • Study Documentation: Ensure the quality and completeness of the Trial Master File (TMF) and other study documents.

  • Project Management: Develop and maintain project plans, track progress, and prepare reports for internal and external stakeholders.

  • Risk Management: Develop and implement risk mitigation strategies and contingency plans to ensure project success.

Business Development

  • Client Relationship Management: Build and nurture strong relationships with current clients to drive future business opportunities.

  • Bid Defense Participation: Support bid defense meetings and may take the lead in presenting project management capabilities.

Management Responsibilities

  • Team Oversight: May be responsible for line managing other project management team members and clinical monitoring staff.


Qualifications

Education and Experience

  • Degree Requirement: A Bachelor’s degree (or equivalent) in Life Sciences, Medicine, Pharmacy, Nursing, or a related field.

  • Clinical Experience: A background in Clinical Research Organization (CRO) work, with significant experience in leading clinical trials, especially in early-phase studies.

  • Regulatory Knowledge: Strong knowledge of GCP/ICH guidelines and relevant regulatory requirements.

Skills

  • Project Management: Strong organizational, time management, and independent work abilities.

  • Leadership: Demonstrated ability to lead cross-functional teams and manage multiple priorities effectively.

  • Communication: Excellent written and verbal communication, with strong presentation and interpersonal skills.

  • Adaptability: Ability to embrace new technologies and adapt to evolving project needs.

Additional Requirements

  • Travel: Ability to travel up to 25% as needed for site visits or meetings.


Compensation & Benefits

  • Salary Range: $85,500 to $175,700 (base salary, depending on experience and qualifications).

  • Benefits: Comprehensive health coverage, 401(k) with company match, Employee Stock Purchase Plan, flexible paid time off (PTO), and more.


Apply Now

If you are a dedicated and experienced project manager with a passion for clinical research, apply today to join the Syneos Health team.

Note: Syneos Health values diversity and encourages all individuals to apply, even if their experience doesn't perfectly match the job description.