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

Syneos Health

6+ years

Not Disclosed

Remote - Europe

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: Czech Republic (CZE) - Home-Based
Job ID: 25001112

Position Overview

Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. Our approach combines clinical, medical affairs, and commercial insights, bringing patients and customers to the forefront of everything we do.

Join us to simplify and streamline processes, making Syneos Health a top choice for employees and clients. With over 29,000 employees in 110 countries, we are passionate about innovation and transforming lives.

Why Join Syneos Health?

Career Growth: Comprehensive development and progression opportunities, therapeutic training, and a supportive management culture.
Inclusive Culture: Authenticity is celebrated through our "Total Self" approach, fostering a global community of belonging.
Diversity and Innovation: We value diverse thoughts, perspectives, and backgrounds, creating an environment where everyone thrives.

Key Responsibilities

Collaboration & Oversight
- Work across multiple departments (Business Development, Clinical, Data Management, etc.) to ensure smooth project execution.
- Address and resolve core issues related to Site Start-Up, regulatory pathways, and patient enrollment.
Project Management
- Manage all deliverables from site identification to activation, including life cycle maintenance.
- Oversee key activities like regulatory submissions, communication with authorities, essential document collection, and trial agreement finalization.
Timelines & Budgets
- Develop detailed start-up timelines, track progress, and proactively manage risks or delays.
- Align budgets with project milestones and ensure profitability, addressing deviations as needed.
Documentation & Strategy
- Prepare submission documents and maintain compliance with SOPs and quality standards.
- Provide updates and strategic guidance during client meetings.
Continuous Improvement
- Contribute to process improvements within the SSU department and lead change initiatives.

Qualifications

Education: Bachelor’s Degree (Higher degree preferred).
Experience:
- Minimum 6 years in CRO industry or 5 years in SSU/clinical trial environments.
- Strong understanding of Phases II-IV clinical trials, ICH-GCP, and EU CTR guidelines.
Skills:
- Excellent communication, presentation, and organizational abilities.
- Proven vendor management and project management expertise.
- Proficiency in negotiating, problem-solving, and guiding peers.

Why Syneos Health Stands Out

Over the last five years, Syneos Health has partnered on 94% of all novel FDA-approved drugs and conducted over 200 studies across 73,000 sites involving 675,000+ trial patients.

Whether driving innovation or challenging the status quo, your role at Syneos Health will make a difference in the competitive, ever-evolving healthcare environment.

Additional Information

This job description is not exhaustive. The company may assign additional responsibilities or tasks as needed, ensuring compliance with relevant regulations such as the EU Equality Directive and ADA standards for reasonable accommodations.

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