Job summary
Job post source
This job is directly from Pharmavise Corporation
Job overview
The Clinical Project Manager leads and manages clinical trials from initiation to closeout, ensuring compliance with regulations and company standards to support successful project delivery.
Responsibilities and impact
The role involves developing and managing clinical trial plans, coordinating cross-functional teams and vendors, ensuring regulatory compliance, monitoring progress and budgets, overseeing vendor performance, preparing reports, supporting audits, and participating in protocol and document development.
Compensation and benefits
The company offers a comprehensive benefits package including paid holidays, Paid Time Off (PTO), and medical insurance to support employee well-being and work-life balance.
Experience and skills
Candidates must have a Bachelor's degree in Life Sciences or related field, at least 5 years of clinical research experience with 2+ years in project management, strong knowledge of GCP and ICH guidelines, experience managing multi-site/global studies, and proficiency with CTMS and Microsoft Office.
Career development
The company fosters a dynamic and collaborative work environment that supports professional and personal growth opportunities.
Work environment and culture
Pharmavise promotes a healthy work-life balance with a supportive and collaborative environment, emphasizing employee well-being.
Company information
Pharmavise Corporation is a clinical research organization focused on managing clinical trials in compliance with regulatory standards and company SOPs.
Job location and travel
This is a remote position, allowing work from any location.
Unique job features
The role includes leadership of multi-site and global clinical trials with involvement in protocol development and regulatory audit readiness, distinguishing it from similar positions.
Company overview
Pharmavise Corporation is a strategic partner for pharmaceutical, medical device, and biotechnology companies, offering expertise in quality, regulatory, and compliance services. Headquartered in Florida, the company supports clients from development to commercialization, ensuring adherence to industry standards. Founded by Ricardo Joseph, Pharmavise employs a team of professionals specializing in drug safety, GMP, and clinical subject matter expertise. The company's commitment to excellence is reflected in its diverse service offerings and its role as a trusted advisor in the life sciences and healthcare sectors.
How to land this job
Tailor your resume to emphasize your experience managing clinical trials from initiation to closeout, highlighting your ability to oversee timelines, budgets, and resource allocation effectively.
Showcase your knowledge of GCP, ICH guidelines, and regulatory compliance, as well as your proficiency with clinical trial management systems (CTMS) and project management tools like MS Project.
Apply through multiple platforms including Pharmavise Corporation's official corporate website and LinkedIn to maximize your application visibility and chances.
Connect with current employees in Pharmavise's clinical research or project management divisions on LinkedIn; start conversations by commenting on recent company news or asking about their experience managing remote clinical projects.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical trial management,' 'regulatory compliance,' 'vendor management,' and 'cross-functional leadership' to pass automated screenings.
Utilize Jennie Johnson's Power Apply feature to automatically tailor your resume, find the best application channels, and identify relevant LinkedIn contacts, freeing you to focus on preparing for interviews and networking.
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