Job summary
Job post source
This job is directly from ProPharma
Job overview
The Senior Clinical Research Associate (Medtech) at ProPharma oversees clinical trial monitoring to ensure compliance and data integrity, playing a key role in advancing medical device and biotech product development.
Responsibilities and impact
The role involves conducting monitoring visits, managing clinical trial sites, reviewing regulatory and trial documentation, communicating with stakeholders, and supporting study start-up and site management activities to ensure proper trial conduct.
Experience and skills
Requires over 5 years of clinical research associate experience, strong communication and organizational skills, proficiency with Microsoft Office and clinical trial systems, and knowledge of regulatory guidelines and GCPs.
Work environment and culture
ProPharma values diversity, equity, and inclusion, promoting an innovative, collaborative, and entrepreneurial work environment where employees can be authentic and empowered.
Company information
ProPharma is a 20-year-old consulting firm specializing in regulatory sciences, clinical research, quality, pharmacovigilance, and R&D technology, supporting biotech, med device, and pharmaceutical clients through the product lifecycle.
Unique job features
The position includes both in-person and remote monitoring responsibilities and involves a broad range of clinical trial management activities across multiple regulatory environments.
Company overview
ProPharma is a global leader in providing comprehensive compliance, regulatory, and quality solutions to the pharmaceutical, biotechnology, and medical device industries. They generate revenue through consulting services, helping companies navigate complex regulatory landscapes, ensuring product quality, and achieving compliance with international standards. Founded in 2001, ProPharma has grown through strategic acquisitions and global expansion, establishing a strong presence in key markets worldwide. Their expertise spans from early development through post-approval, making them a trusted partner in bringing safe and effective products to market.
How to land this job
Position your resume to highlight extensive experience in clinical research monitoring, emphasizing your ability to conduct site visits, both in-person and remote, and your proficiency in monitoring report writing within regulatory guidelines.
Emphasize your knowledge of regulatory requirements, ICH Guidelines, GCPs, and experience with EDC, CTMS, IVRS, and eTMF systems, as these are critical for the Senior Clinical Research Associate role at ProPharma.
Apply through multiple channels such as ProPharma's corporate career site and LinkedIn to maximize your visibility and chances of being noticed for this position.
Connect with current employees in ProPharma's clinical research or medtech divisions on LinkedIn; use ice breakers like commenting on recent ProPharma projects, asking about their experience with clinical monitoring tools, or expressing enthusiasm for the company's commitment to innovation and diversity.
Optimize your resume for ATS by incorporating key phrases from the job description like 'clinical monitoring,' 'regulatory compliance,' 'site initiation,' 'source document review,' and 'investigational supplies management' to ensure it passes automated screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailored resume submissions, identify multiple application portals, and find relevant LinkedIn contacts, allowing you to focus your energy on preparing for interviews and networking effectively.
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