Job summary
Job post source
This job is directly from Pharmavise Corporation
Job overview
The Clinical Research Manager at Pharmavise Corporation oversees clinical trials across various phases, ensuring compliance and managing cross-functional teams to drive successful study execution.
Responsibilities and impact
The CRM leads planning and management of clinical trials, oversees site selection, patient recruitment, compliance, budgeting, team supervision, vendor management, and reporting to senior leadership.
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
Requires a Bachelor's degree in Life Sciences or related field, 5-7 years clinical research experience with 2+ years in management, knowledge of ICH-GCP, clinical trial software proficiency, and ability to travel up to 20%.
Career development
The role provides opportunities for professional growth within a dynamic and collaborative environment supporting both personal and career development.
Work environment and culture
Pharmavise fosters a healthy work-life balance with a dynamic and collaborative work environment focused on employee well-being.
Company information
Pharmavise Corporation is a clinical research organization involved in managing multi-phase clinical trials with a focus on regulatory compliance and quality standards.
Team overview
The CRM manages cross-functional teams including CRAs, CTAs, study coordinators, and collaborates with regulatory, data management, biostatistics, and medical writing teams.
Job location and travel
This is a remote position with up to 20% travel required.
Unique job features
The role involves managing diverse clinical trial phases and therapeutic areas with extensive vendor and CRO coordination, emphasizing regulatory compliance and leadership.
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 leadership in managing Phase I-IV clinical trials, emphasizing your strategic oversight and compliance with FDA and ICH-GCP guidelines as required by Pharmavise Corporation.
Showcase your experience in cross-functional team management, vendor and CRO relationship oversight, and your ability to handle project timelines and budgets effectively, which are key responsibilities for the Clinical Research Manager role.
Apply through multiple channels including Pharmavise Corporation’s official corporate careers page and LinkedIn to maximize your application visibility for this remote position.
Connect on LinkedIn with current Clinical Research Managers, project leads, or HR personnel at Pharmavise Corporation; use ice breakers such as commenting on recent Pharmavise clinical trial successes, asking about team culture in remote settings, or inquiring about challenges in multi-therapeutic area trials to start meaningful conversations.
Optimize your resume for ATS by incorporating keywords from the job description like 'clinical trials management,' 'ICH-GCP compliance,' 'vendor management,' 'project timelines,' and 'clinical trial software' to ensure your resume passes initial screenings.
Leverage Jennie Johnson’s Power Apply feature to automate tailored resume optimization, identify the best application platforms, and find relevant LinkedIn contacts, allowing you to focus your time on interview preparation and networking.
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