Nurse Practitioner / Physician Assistant

ActivMed Practices & Research, LLC.; Fredericksburg (VA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k with match

Health savings accounts

Job summary

Alcanza Clinical Research in the United States seeks a Sub Investigator / Clinical Research Coordinator to support multiple sites across Phase I–IV studies. You will implement IRB-approved protocols, supervise data collection, and ensure patient safety under the Principal Investigator's direction.

Preferred candidates hold a Master’s degree with 2+ years of clinical research experience, an active state license, and BLS/ACLS certification; bilingual English/Spanish is a plus.

Qualifications

• Master's degree and 2+ years of clinical experience.
• Active license to practice in the state of practice is required.
• BLS/ACLS certification required; bilingual English/Spanish a plus.

Responsibilities

• Perform Sub Investigator duties under the Principal Investigator's direction.
• Ensure IRB-approved protocols are implemented and followed.
• Execute informed consent process and monitor patient safety.
• Assist with site initiation visits and training as needed.
• Maintain HIPAA compliance and protect confidentiality.

Skills

Communication skills

Interpersonal skills

Time management

Detail orientation

HIPAA compliance

Typing 40+wpm

Proficiency with MS Office

Education

Master's degree

Active clinical license

BLS/ACLS certification

Tools

Electronic Health Records

MS 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.

Essential Job Duties

• Under the direction of the Principal Investigator, performs the functions of Sub Investigator on research studies. Ensures IRB approved protocols are implemented and followed. Executes informed consent process and monitors patient status and safety; collects and organizes research data; schedules and conducts study specific training and site in-services to study related staff on new or amended protocols; educates patients and their families about treatments and possible side effects. Ensure and protect the patient’s welfare and rights as a research subject.
• May perform research protocol procedures which may include, but are not limited to: physical exams, injections, IVs, medical history review and assessment, and assessments of vital signs, laboratory results and adverse events. May mix and/or dispense investigational product and instruct subjects on usage and potential drug interactions;
• Participates at pre-study and site initiation visits, investigator meetings, and other customer facing meetings, as needed;
• Assist site management with support in change management and process improvement;
• Assist and participate with new staff training and mentoring;
• Assist and guide employees on study specific tasks;
• Utilize and ensure the appropriate equipment is on-site for Universal Precautions for themselves and others in and around areas that may contain potential biohazards
• Work with the Principal Investigator to maintain high quality and patient safety.
• Establish rapport with sponsor representatives and maintain frequent face-to-face, written and telephone contact with various persons involved in the study, including but not limited to the patients, relatives/friends of the patients, doctors, pharmaceutical sponsors and all levels of the company;
• May perform role of Clinical Research Coordinator on studies as needed.
• Maintain strict confidentiality of patients, employees and company information at all times and adheres to HIPAA Guidelines;
• Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;
• Adhere to GCP, ICH, HIPAA, NIH, FDA Regulations and SOPs and maintain ongoing regulatory documents;
• Practical knowledge of document processes and reporting of SAEs, 1572s, CRFs, ICFs, etc.;
• Maintain accountability of own ongoing professional growth and development;
• Performing all other duties as requested or assigned.

Minimum Qualifications: A Master's degree and a minimum of 2 years of clinical experience. Active license (in good standing) to practice as an advanced practice professional in the state of practice is required. Research experience is plus. BLS/ACLS certified required. Bi-lingual (English / Spanish) proficiency is a plus.

Required Skills

• Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications
• Ability to type proficiently (40+ wpm);
• Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, reconstitution of IP, injections, and IV’s.
• 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 work under minimal supervision, identify problems and implement solutions.
• 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

Alcanza Clinical Research (“Alcanza”) 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.