Syneos Health

Sponsor Dedicated Senior Start Up and Regulatory Specialist - Home Based Israel

REMOTEPosted 20 days ago

Job summary

  • Job post source

    This job is directly from Syneos Health

  • Job overview

    The Sponsor Dedicated Senior Start Up and Regulatory Specialist role at Syneos Health focuses on managing clinical trial start-up activities and regulatory submissions to ensure compliance and timely approvals, impacting clinical research success.

  • Responsibilities and impact

    The specialist will manage start-up activities for clinical trials, prepare and submit clinical trial applications, follow up on approvals, maintain communication with health authorities, manage document translations and approvals, and ensure regulatory compliance.

  • Experience and skills

    Candidates should have a bachelor's degree in life sciences or related fields, basic GCP qualification, at least 2 years of experience in start-up or regulatory roles in clinical trials, and fluency in Hebrew and English.

  • Career development

    Syneos Health emphasizes career development, progression, technical and therapeutic training, and peer recognition to support employee growth.

  • Work environment and culture

    The company promotes a Total Self culture valuing diversity, inclusion, and a supportive work environment where employees can be authentic and engaged.

  • Company information

    Syneos Health is a leading biopharmaceutical solutions organization with 29,000 employees across 110 countries, known for its integrated clinical development model and extensive work with FDA and EMA approved drugs.

  • Job location and travel

    This is a home-based position located in Israel.

  • Unique job features

    The role offers the opportunity to work in a fully integrated biopharmaceutical company with a focus on accelerating therapy delivery and collaborating in a team-driven environment.

Company overview

Syneos Health is a leading biopharmaceutical solutions organization that provides comprehensive clinical and commercial services. They make money by partnering with pharmaceutical, biotechnology, and healthcare companies to bring innovative therapies to market, offering services such as clinical trials management, regulatory consulting, and commercial strategy. Founded in 2018 through the merger of INC Research and inVentiv Health, Syneos Health has a rich history of combining clinical expertise with commercial insights to accelerate customer success. Their integrated approach helps streamline the drug development process, ultimately improving patient outcomes.

How to land this job

  • Position your resume to highlight your experience managing clinical trial start-up activities, emphasizing compliance with local regulations, GCP, and regulatory submissions relevant to Israel.

  • Focus on showcasing your ability to prepare and submit Clinical Trial Applications, maintain communication with Health Authorities and Ethics Committees, and handle document translations and approvals.

  • Apply through multiple platforms including Syneos Health's corporate career site, LinkedIn, and specialized clinical research job boards to maximize your chances.

  • Connect on LinkedIn with professionals in Syneos Health's clinical development or regulatory affairs teams based in Israel; start conversations by mentioning your interest in their work on local regulatory submissions or asking about recent clinical trial start-up challenges they have faced.

  • Optimize your resume for ATS by incorporating keywords such as 'clinical trial applications,' 'regulatory submissions,' 'start-up specialist,' 'GCP,' 'Health Authorities,' and 'Ethics Committees' to ensure it passes automated screenings.

  • Use Jennie Johnson's Power Apply feature to automate submitting tailored applications across multiple job boards and identify LinkedIn contacts, freeing you to focus on networking and interview preparation.

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