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Site Activation Managers, Sponsor Dedicated. Oncology Exp Essential. Homebased

6+ years
Not Disclosed
10 Jan. 16, 2025
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

Site Activation Manager - Sponsor Dedicated (Oncology Experience Essential)

Updated: Yesterday
Location: Greece (GRC) - Home-Based
Job ID: 25001112


Position Overview

Syneos Health® is a fully integrated biopharmaceutical solutions organization that focuses on accelerating customer success. We are committed to improving lives through our Clinical Development model, which centers on the customer and the patient, continuously refining processes to streamline our work and make Syneos Health easier to work with.

Whether you work in a Functional Service Provider partnership or a Full-Service environment, you'll join a passionate team that is innovative, agile, and driven to deliver life-changing therapies.

WORK HERE MATTERS EVERYWHERE.


Why Join Syneos Health?

  • Career Growth: Career development and progression, supported by engaged line management, technical training, and a peer recognition program.
  • Inclusive Culture: Our Total Self culture promotes authenticity and inclusivity across the organization.
  • Diversity & Innovation: A diverse and collaborative environment where everyone feels they belong.

Key Responsibilities

  1. Collaboration & Oversight

    • Work alongside Business Development, Project Management, Clinical, and other teams to ensure successful project activation and delivery.
    • Identify and address issues related to site start-up, regulatory pathways, and patient enrollment.
  2. Site Start-Up Management

    • Oversee the entire site start-up process, from site selection to activation and lifecycle maintenance.
    • Manage regulatory activities, clinical trial agreements, investigator budgets, and documentation.
  3. Budget & Timeline Management

    • Develop and manage integrated site start-up timelines.
    • Ensure that projects meet profitability targets and take corrective actions when necessary to maintain budget alignment.
  4. Documentation & Strategy

    • Prepare and review clinical trial documents, ensuring compliance with quality standards.
    • Present site start-up strategies and status updates to clients and internal teams.
  5. Continuous Improvement

    • Contribute to initiatives that drive improvements within the SSU department.

Qualifications

  • Education: Bachelor’s Degree (Higher degree preferred).
  • Experience:
    • Minimum of 6 years in the CRO industry or 5 years in clinical trial/SSU environments.
    • Expertise in Phases II-IV clinical trials, ICH GCP, and EU CTR guidelines.
  • Skills:
    • Excellent communication and organizational skills.
    • Proven ability to handle multiple projects under pressure.
    • Strong vendor management and problem-solving skills.

Why Syneos Health Stands Out

Syneos Health has supported the development of 94% of FDA-approved drugs and 95% of EMA-authorized products in the last 5 years. Join us in a challenging and competitive environment that will allow you to make a significant impact on clinical trials.


Additional Information

This job description is not exhaustive, and Syneos Health reserves the right to adjust tasks and responsibilities as necessary. We are committed to providing reasonable accommodations for applicants with disabilities.