Alcanza Clinical Research

Inclusive clinical trials for diverse patients

Clinical Research Physician - Internal Medicine

Physicians & SurgeonsUpdated on Nov 13

Part-timeKansas City, MO, USANo salary listedIn-person

About the Job

Requirements

An MD or DO degree is required.
An active physician license in good standing in the state of practice is required.
Experience with clinical trials is required.
Board certification in the area of specialty is required.
Clinical skills and clinical procedures based in the area of specialty are required.
Proficiency with computer applications such as Microsoft Office, electronic health records, and web applications is required, as is the ability to type at least 40 words per minute.
Strong organizational skills, attention to detail, and math proficiency are required.
Written and verbal communication skills are required.
Interpersonal and listening skills and the ability to work effectively independently and with coworkers, employees, study subjects, managers, and external customers are required.
The ability to handle multiple tasks and adapt to changes in workloads and priorities is required.
The ability to work independently to identify problems and implement solutions is required.
The ability to handle highly sensitive information confidentially and professionally and in compliance with HIPAA guidelines is required.
CPR certification is required.

Responsibilities

Conduct and coordinate daily clinical trial activities according to ICH, FDA, and GCP guidelines, local regulations, study protocols, and company policies and processes.
Work with local and central teams to provide clinical oversight and ensure the quality of assigned studies at the site.
Ensure the medical well-being and safety of study participants through the safe performance and ethical execution of clinical trials, adhering to FDA, ICH, NIH, GCP, and HIPAA guidelines, study protocols, and company policies and processes.
Provide overall site leadership focused on improving efficiencies, patient safety, and protocol, GCP, and regulatory compliance.
Evaluate and assess participants to ensure that only eligible participants enroll in trials.
Participate in and contribute to the successful delivery and retention of study participants.
Interact positively and collaboratively with sponsors, clients, and team members.
Record data and participant information accurately in accordance with protocol guidelines and GCPs.
Participate actively in protocol training for staff.
Participate in Investigator Meetings and continuing education activities to maintain current knowledge of recruitment affairs and issues.
Perform other duties as assigned, requested, or required based on the needs of participants, protocols, or the company.

Desired Qualifications

Proficiency in both English and Spanish is highly preferred.
ACLS certification is preferred.

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.

The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.

Essential Job Duties:

Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
Participates and engages in successful delivery and retention of study participants.
Interacts positively and collaboratively with sponsors, clients and team members.
Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
Actively involved in protocol training for staff.
Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.

Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role. Experience with clinical trials required. Board certification in area of specialty is required. CPR required / ACLS preferred.

Required Skills:

Clinical skills and clinical procedures based in area of specialty.
Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
Must possess strong organizational skills, attention to detail, and math proficiency.
Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred.
Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.
Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.
Must possess a high degree of urgency, self-motivation, integrity and dependability.
Ability to work independently to identify problems and implement solutions.
Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

About the Company

Alcanza Clinical Research

Inclusive clinical trials for diverse patients

Alcanza Clinical Research conducts inclusive clinical trials by partnering with pharmaceutical companies, medical providers, and community organizations to enroll diverse patient populations across major therapeutic areas. Its studies follow established protocols with certified research professionals to ensure patient safety and data integrity, while participants may receive health tests and access to emerging treatments at no cost. The company differentiates itself through active community collaboration, broad patient diversity, and education alongside trial execution, expanding trial reach. Its goal is to speed the development of new therapies by removing participation barriers and delivering high-quality, diverse clinical research.

Company size: 201-500
Company stage: Not listed
Total funding: Not listed
Headquarters: Lake Mary, FL
Founded: 2021

Recently Posted Jobs

Explore more opportunities at Alcanza Clinical Research

See more jobs