Job summary
Job post source
This job is directly from Pharmavise Corporation
Job overview
The Clinical Research Associate (CRA) role at Pharmavise Corporation supports ongoing clinical research projects by managing study maintenance and closeout activities to ensure efficient project execution.
Responsibilities and impact
The CRA will oversee study-level project management tasks such as study maintenance, data lock, closeout, document review, and budget monitoring, act as the primary liaison between internal teams and external partners, track safety and clinical data, manage clinical queries, and coordinate with business partners to ensure compliance with study requirements.
Compensation and benefits
The position 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, 6+ years in clinical research or related fields, 3+ years in project management, experience with clinical trial management tools, knowledge of GCP guidelines, and strong organizational and communication skills.
Career development
The job description mentions support for professional and personal growth within a dynamic and collaborative work environment.
Work environment and culture
Pharmavise promotes a healthy work-life balance with a dynamic and collaborative environment supporting employee well-being.
Company information
Pharmavise Corporation is involved in clinical research, focusing on pharmaceutical, diagnostics, or CRO environments, emphasizing regulatory compliance and clinical operations.
Job location and travel
This is a remote position allowing flexibility in work location.
Unique job features
The role is distinguished by its focus on surge capacity support for ongoing studies, emphasizing study maintenance and closeout rather than study startup activities.
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 highlight your extensive experience in clinical research, particularly focusing on study maintenance, closeout activities, and project management skills as emphasized by Pharmavise Corporation.
Emphasize your proficiency with clinical trial management tools such as Medidata RAVE, Veeva Vault, Oracle InForm, and your familiarity with eTMF systems, query management, and safety reporting databases to match the job requirements.
Apply through multiple channels including Pharmavise Corporation's official corporate website and LinkedIn to maximize your chances of being noticed for the Clinical Research Associate role.
Connect with current employees or team members in the clinical research division at Pharmavise Corporation on LinkedIn; use ice breakers like commenting on recent company projects, asking about their experience with clinical trial management tools, or expressing interest in how they manage study closeout processes.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical research associate,' 'study maintenance,' 'project management,' 'Medidata RAVE,' 'Veeva Vault,' 'GCP guidelines,' and 'regulatory compliance' to ensure it passes automated screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailoring your resume, applying through multiple platforms, and identifying LinkedIn connections to network with, allowing you to focus your time on preparing for interviews and enhancing your clinical research expertise.
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