Job summary
Job post source
This job is directly from Pharmaron
Job overview
The Clinical Research Nurse at Pharmaron in Baltimore leads and supports clinical research activities, ensuring participant safety and protocol compliance to contribute to impactful biopharmaceutical studies.
Responsibilities and impact
The nurse coordinates staff assignments, guides participants through study protocols, manages informed consent, performs clinical procedures, monitors safety, maintains protocol compliance, collaborates with clinical teams, mentors staff, and upholds privacy and regulatory standards.
Compensation and benefits
The position offers an hourly wage of $48.00 to $57.00, medical, dental, and vision insurance with employer contributions, employer-funded health reimbursement account, flexible spending accounts, life and disability insurance fully paid by employer, a 401k plan with employer match, and access to an employee assistance program.
Experience and skills
Candidates must have a BSN, active Maryland RN license, ACLS certification or ability to obtain it within 3 months, experience with IVs, phlebotomy, investigational product administration, knowledge of GCP, ICH, and FDA regulations, strong time management, communication, leadership skills, and preferably clinical research experience.
Career development
Pharmaron offers growth opportunities in a collaborative environment with a focus on innovation and employee development within the life sciences R&D sector.
Work environment and culture
Pharmaron promotes an inclusive, collaborative culture valuing teamwork, innovation, employee well-being, and diversity, emphasizing employee and client-centered values.
Company information
Pharmaron is a global R&D service provider in life sciences founded in 2004, with over 19,000 employees and operations in China, the U.S., and the U.K., specializing in drug discovery and clinical development across multiple therapeutic modalities.
Team overview
The Clinical Research Nurse will join a dynamic clinical research team in Baltimore working collaboratively to support biopharmaceutical research studies.
Job location and travel
The job is located in Baltimore, Maryland, with a rotating schedule of three 12-hour shifts per week.
Application process
Applicants are instructed to apply online through Pharmaron's website, with the company emphasizing equal employment opportunity and diversity.
Unique job features
This role uniquely combines clinical nursing with research responsibilities in a fast-paced, team-oriented environment, offering the chance to impact global biopharmaceutical studies directly.
Company overview
Pharmaron is a global contract research organization (CRO) that provides comprehensive R&D services to the pharmaceutical and biotech industries. They generate revenue by offering services across the drug discovery, preclinical, and clinical development stages, including chemistry, biology, pharmacology, and manufacturing. Founded in 2004 in Beijing, Pharmaron has expanded its operations worldwide, establishing a significant presence in the U.S., U.K., and China. Key historical milestones include its IPO on the Shenzhen Stock Exchange in 2019 and strategic acquisitions to enhance its service capabilities.
How to land this job
Position your resume to highlight your RN licensure in Maryland, your experience with IVs, phlebotomy, and investigational product administration, and your familiarity with GCP, ICH Guidelines, and FDA regulations to align with Pharmaron's Clinical Research Nurse role.
Emphasize leadership skills by detailing experience coordinating clinical staff, mentoring team members, and managing clinical shifts, as these are key responsibilities in this position.
Apply through multiple platforms including Pharmaron's official corporate careers page and LinkedIn to maximize your application visibility and increase chances of being noticed.
Connect with current Clinical Research Nurses or team leads at Pharmaron on LinkedIn, using ice breakers like commenting on recent clinical trials Pharmaron has conducted or expressing enthusiasm about contributing to global-impact research.
Optimize your resume for ATS by incorporating exact keywords from the job description such as 'clinical protocol compliance,' 'participant safety,' 'investigational product administration,' 'GCP,' and 'ICH Guidelines' to ensure your resume passes screening filters.
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