Job summary
Job post source
This job is directly from Pharmavise Corporation
Job overview
The Clinical Subject Matter Expert role at Pharmavise Corporation involves providing expert clinical guidance to support and optimize clinical development programs, impacting patient safety and regulatory compliance.
Responsibilities and impact
The role includes reviewing clinical trial protocols, providing strategic input on trial design, monitoring trials for compliance and safety, analyzing trial data, collaborating with cross-functional teams, staying updated on clinical research advancements, and representing the company externally.
Compensation and benefits
Competitive compensation packages are offered; specific salary details and benefits are not provided.
Experience and skills
Candidates must have an advanced medical degree (MD) or equivalent, at least 5 years of clinical research experience, strong knowledge of clinical trial design and regulatory requirements, leadership skills, and excellent communication abilities; certifications like RAC, CCRA, or CPI are preferred but not required.
Career development
The position offers opportunities to shape and drive clinical development programs across multiple therapeutic areas, implying potential for professional growth and leadership within the company.
Work environment and culture
Pharmavise values excellence through quality and promotes an inclusive, equal opportunity work environment with a focus on compliance and patient safety.
Company information
Pharmavise Consulting Corp. is a regulatory compliance consulting firm partnering with pharmaceutical, medical device, and biotechnology clients to address complex compliance issues and improve patient health and safety.
Job location and travel
This is a remote position, allowing work from any location.
Unique job features
The role is pivotal within the organization, offering unique opportunities to influence clinical programs and represent the company at scientific and regulatory forums.
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 advanced medical degree and clinical expertise, highlighting your experience in clinical trial design, execution, and regulatory compliance with GCP and ICH E6(R2) guidelines.
Showcase your leadership skills and experience collaborating with cross-functional teams such as clinical operations, regulatory affairs, and biostatistics to demonstrate your ability to drive clinical programs to success.
Apply through multiple channels including Pharmavise Corporation’s official corporate website and LinkedIn to maximize your application’s visibility and ensure you meet all submission requirements.
Connect with professionals in Pharmavise’s clinical or regulatory divisions on LinkedIn; initiate conversations by referencing recent Pharmavise projects, industry trends, or asking about their experience with clinical trial innovations to break the ice.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical trial design,' 'regulatory compliance,' 'patient safety,' 'data integrity,' and 'clinical development programs' to pass automated screening effectively.
Utilize Jennie Johnson’s Power Apply feature to automate tailored resume customization, identify multiple application portals, and find relevant LinkedIn contacts, allowing you to focus more on preparing for interviews and networking.
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