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

6+ years

Not Disclosed

Madrid

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: Spain (ESP) - Home-Based (Madrid)
Job ID: 25001112

Position Overview

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. With a Clinical Development model that places the customer and patient at the heart of everything we do, we continuously strive to streamline processes for more efficient collaboration.

Joining Syneos Health means being part of a team dedicated to accelerating the delivery of life-saving therapies and contributing to impactful change.

WORK HERE MATTERS EVERYWHERE.

Why Join Syneos Health?

Career Growth: Career development, training, and recognition programs designed for your progression.
Inclusive Culture: Our Total Self culture emphasizes authenticity, diversity, and inclusion, uniting employees globally.
Engaged Leadership: Supportive line management and a collaborative work environment.

Key Responsibilities

Collaboration & Oversight
- Coordinate with Business Development, Project Management, Clinical, and other functional teams to ensure effective project delivery.
- Address issues related to site start-up, regulatory paths, and patient enrollment, implementing solutions.
Site Start-Up Management
- Oversee activities from site selection to activation and lifecycle management.
- Ensure compliance with regulatory requirements, clinical trial agreements, and investigator budgets.
Budget & Timeline Management
- Develop and manage timelines, tracking progress and addressing risks or gaps.
- Work with project leads to ensure profitability and address corrective measures when necessary.
Documentation & Strategy
- Prepare clinical trial documents, ensuring compliance with quality standards.
- Present site start-up strategies and provide updates to clients and internal teams.
Continuous Improvement
- Contribute to change initiatives across the Site Start-Up department.

Qualifications

Education: Bachelor’s Degree (Higher degree preferred).
Experience:
- Minimum 6 years of experience in CRO or 5 years in SSU/clinical trials environments.
- Knowledge of Phases II-IV trials, ICH GCP, and EU CTR.
Skills:
- Strong communication, organizational, and problem-solving abilities.
- Project management experience, vendor management, and quality-driven work.

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. Be part of a company that challenges the status quo and drives significant change in clinical trials.

Additional Information

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

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

Job Description

Site Activation Manager - Sponsor Dedicated (Oncology Experience Essential)

Position Overview

Why Join Syneos Health?

Key Responsibilities

Qualifications

Why Syneos Health Stands Out

Additional Information

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