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Job summary
Job post source
This job is directly from Syneos Health.
Job overview
The FSP Pfizer CRA role at Syneos Health involves monitoring clinical research studies to ensure compliance and quality, significantly impacting the integrity and success of clinical trials.
Responsibilities and impact
The role includes conducting on-site and remote monitoring, developing monitoring tools and procedures, managing project components, documenting activities, and collaborating with cross-functional teams to support clinical trial operations.
Experience and skills
Candidates need a bachelor's degree or equivalent experience, 2-4 years in clinical research monitoring, strong GCP knowledge, communication skills, ability to manage priorities, proficiency in clinical trial systems, and preferably a CCRA certification.
Career development
Syneos Health emphasizes career development through training, progression opportunities, and supportive management, fostering growth within a global biopharmaceutical environment.
Work environment and culture
The company promotes a Total Self culture valuing diversity, inclusion, and employee well-being, aiming to create a supportive and engaging workplace.
Company information
Syneos Health is a leading integrated biopharmaceutical solutions organization with 29,000 employees across 110 countries, known for its work with FDA-approved drugs and extensive clinical trials.
Job location and travel
The position is based in the Netherlands with potential for on-site and remote work related to clinical trial monitoring.
Unique job features
The role offers the opportunity to work on innovative clinical trial processes and contribute to advancing medical knowledge and patient outcomes.
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 with clinical research monitoring, emphasizing your knowledge of Good Clinical Practice (GCP) guidelines and regulatory compliance relevant to Syneos Health's standards.
Focus on showcasing your skills in developing and implementing monitoring tools, procedures, and processes, as well as your ability to manage clinical trial components and coordinate with cross-functional teams.
Apply through multiple platforms including Syneos Health's official corporate website and LinkedIn to maximize your visibility and chances of being noticed for the FSP Pfizer CRA role.
Connect with current employees in the Clinical Monitoring or CRA division at Syneos Health on LinkedIn; start conversations by mentioning your interest in their recent projects or asking about their experience working on Pfizer-related trials to break the ice.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical research monitoring,' 'GCP,' 'monitoring plans,' 'clinical trial management systems,' and 'regulatory compliance' to ensure it passes initial screenings.
Utilize Jennie Johnson's Power Apply feature to automate applying across multiple job boards, tailor your resume for ATS optimization, and identify LinkedIn connections to network with, allowing you to spend your job search time more effectively.