Clinical Research Physician - Internal Medicine

Alcanza Clinical Research; Woodstock (GA); Sur place; USD 180 000 - 240 000; Plein temps

Avantages offerts par ce poste

Medical, dental, vision coverage

401k with safe harbor match

Résumé du poste

Alcanza Clinical Research, LLC in Woodstock, GA is seeking an MD/DO Principal Investigator to lead daily clinical trial activities at the North Georgia site in accordance with ICH/FDA/GCP guidelines and approved protocols. The PI will oversee staff, ensure participant safety, monitor compliance, and collaborate with sponsors to maintain data quality and trial timelines while upholding HIPAA standards.

Strong clinical, organizational, and bilingual English/Spanish communication skills are

Qualifications

• MD or DO degree with active license in the state of practice.
• Board certification in specialty required.
• Clinical research experience preferred.

Responsabilités

• Leads daily clinical trial activities per ICH/FDA/GCP and protocol.
• Ensures participant safety and trial data integrity.
• Oversees staff and coordinates with sponsors and sites.
• Maintains regulatory compliance and HIPAA standards.
• Engages in investigator meetings and ongoing training.
• Performs duties as assigned to support trial needs.

Connaissances

Clinical skills

MS Office

Electronic health records

Typing 40 wpm

Organizational skills

Written and verbal communication

Bilingual English/Spanish

Interpersonal skills

HIPAA compliance

Formation

MD or DO degree

Active physician license

Board certification in specialty

Outils

MS Office

Electronic health records

Description du poste

Key Responsibilities

Department: Operations
Location: North Georgia Clinical Research - Woodstock, GA
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.
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.
Key Responsibilities
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.

Skills, Knowledge And Expertise
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required. Experience in clinical research is preferred. Board certification in area of specialty is required.
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.

Benefits

• 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.