Lab Coordinator / Phlebotomist

ActivMed Practices & Research, LLC.; Charleston (SC); On-site; USD 42,000 - 56,000; Full time

Benefits offered by this job

Health insurance

401k with safe harbor match

Short and long-term disability

Job summary

Alcanza Clinical Research is seeking a Lab Coordinator to execute lab procedures per GCP, ICH, FDA/HIPAA guidelines and company SOPs. You will draw and process specimens, monitor inventory, and support shipments to central labs.

Minimum 1 year in clinical laboratory processing is required; Associates degree preferred. Bilingual English/Spanish is a plus; full-time with benefits offered.

Qualifications

• High School diploma or equivalent and a minimum of 1 year of clinical laboratory processing experience.
• Associates degree is preferred.
• Bilingual (English/Spanish) skills are a plus.

Responsibilities

• Draw and process specimens according to trial requirements.
• Assist with specimen shipments to central labs and ensure proper shipping methods.
• Monitor expiration dates on lab equipment and supplies.
• Unpack and put away incoming lab supplies.
• Maintain general and study-specific lab inventory.
• Transport samples.
• Mentor new hires and allow shadowing.
• Complete and renew GCP/IATA training as required.
• Attend SIVs and sponsor-required lab training.
• Support other clinical research activities as needed.
• Ensure compliance with HIPAA and FDA regulations.

Skills

Typing 40+ wpm

Organizational skills

Written & verbal communication

Interpersonal skills

Multitasking

Professional & ethical

HIPAA compliance

Education

Associates degree preferred

Tools

EHR systems

Web applications

Microsoft Office

Job description

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

Lab Coordinator

The Lab Coordinator works to ensure the execution of assigned lab procedures in compliance with GCP, ICH, FED and HIPAA regulations, company SOPs, and policies.

Essential Job Duties

• Draw and process specimens according to each trial’s requirements
• Assist with specimen shipments to central labs and ensure proper shipping methods have been observed
• Monitor expiration dates on lab equipment and supplies
• Unpack and put away incoming lab supply shipments
• Monitor and maintain both general and study-specific lab inventory, and ensure study-specific lab supplies are ready for new study start-up
• Transport samples
• Provide mentoring to new hires and allow them to shadow you as they learn.
• Complete and renew CITI GCP and IATA training as required.
• Attend SIVs when needed, and complete all sponsor-required lab training.
• May support other clinical research-related activities such as recruitment, EDC and QA/Chart review as needed.
• Ensuring compliance with company SOPs, FDA/HIPAA regulations, ICF documentation, and GCP guidelines
• Maintaining confidentiality of patients, customers, and company information
• Performing other related activities as assigned.

Minimum Qualifications

High School diploma or equivalent and a minimum of 1 year of clinical laboratory processing experience is required. Associates degree is preferred. Bilingual (English/Spanish) skills are a plus.

Required Skills

• Proficiency with computer applications such as Microsoft applications, email, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
• Strong organizational skills and attention to detail.
• Well-developed written and verbal communication skills.
• Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
• Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
• Must be professional, respectful of others, self-motivated, and have a strong work ethic.
• Must possess a high degree of integrity and dependability.
• Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
• Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
• Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

Alcanza Clinical Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all.

We conduct research on dozens of conditions in several therapeutic areas including psychiatry, neurology, dermatology, and infectious disease. Our work is important to the patients who participate, the scientists who develop these new therapies, and the entire medical community. Because all approved medications require clinical trials, the impact of your work is exponential, reaching many thousands of future patients and improving their quality of life.

Alcanza is a culturally competent organization. We treat each other with dignity, creating an environment where all individuals feel welcome, heard, and respected for their unique perspectives and aspirations. We put considerable effort into finding exceptional employees who mirror the values most important to us: Inclusive, Impactful, Compassionate, and Determined.

Alcanza Clinical Research is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, marital status, veteran status, disability, sexual orientation, gender identity or expression, genetic information, or any other category protected by law. We recognize that diversity and inclusion is a driving force in the success of our company.