Job summary
Job post source
This job is directly from Green Life Science
Job overview
The Clinical Research Coordinator II at Green Life Science manages and coordinates clinical trials to ensure participant safety and regulatory compliance, playing a key role in high-quality investigational research.
Responsibilities and impact
The role involves supporting the Principal Investigator, managing study startup activities, conducting study visits and procedures, overseeing informed consent, ensuring accurate documentation, screening participants, maintaining regulatory files, preparing for audits, collaborating with teams, mentoring junior staff, and contributing to recruitment strategies.
Experience and skills
Candidates must have a Bachelor's degree in life sciences, at least 5 years of site-based clinical research coordination experience, 2 years of mentoring experience, certifications in GCP, IATA, ALCOAC, and BLS/CPR certification or willingness to obtain it, along with strong knowledge of clinical trial processes and excellent communication skills.
Company information
Green Life Science is a growing clinical research site focused on conducting high-quality investigational trials with a commitment to regulatory compliance and participant safety.
Team overview
The candidate will join a clinical research team working closely with Principal Investigators and cross-functional staff including pharmacy, regulatory, and clinical personnel.
Job location and travel
Full-time onsite position at a clinical research site, indicating a physical work environment.
Unique job features
The role offers involvement in all phases of clinical trial coordination from startup to closeout, including mentoring junior staff and contributing to recruitment and retention strategies.
Company overview
Green Life Science is a company focused on developing sustainable and eco-friendly solutions in the biotechnology sector. They make money by creating innovative products and technologies that promote environmental conservation and address global challenges such as pollution and climate change. The company has a history of pioneering research in green technologies and has established partnerships with various environmental organizations to enhance its impact. Green Life Science is committed to advancing scientific knowledge while maintaining a strong emphasis on sustainability and ethical practices.
How to land this job
Tailor your resume to highlight your 5+ years of site-based clinical research coordination experience, emphasizing your expertise in regulatory compliance, participant safety, and study startup through closeout.
Focus on showcasing your skills in managing study visits, informed consent processes, data entry accuracy, and adverse event reporting, as these are critical for the Clinical Research Coordinator II role at Green Life Science.
Apply through Green Life Science's corporate career site and LinkedIn, as submitting applications across multiple platforms increases your visibility and chances of being noticed.
Connect with current Clinical Research Coordinators or team members in Green Life Science’s clinical research division on LinkedIn; use ice breakers like asking about their experience with recent trial protocols or how they manage compliance challenges in their role.
Optimize your resume for ATS by incorporating keywords from the job description such as 'regulatory compliance,' 'study startup,' 'participant safety,' 'GCP,' 'ALCOAC,' and 'clinical trial workflows' to ensure your resume passes initial screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailored applications across multiple job boards and identify relevant LinkedIn contacts for networking, allowing you to focus more on preparing for interviews and skill enhancement.
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