Clinical Research Physician

Alcanza Clinical Research; Woodstock (GA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical and dental insurance

401k plan with a match

Short and long-term disability insurance

Job summary

A growing multi-site clinical research company is seeking a Principal Investigator to lead and coordinate clinical trial activities. The role includes ensuring the safety of study participants and evaluating their eligibility. Candidates must have an MD or DO degree, an active physician license, and at least 2 years of experience in medical research. Benefits include medical, dental, vision, and a 401k plan. The position is full-time and offers a mid-senior level career path with various health benefits.

Qualifications

• Active physician license in good standing required.
• Minimum of 2 years experience in a medical research environment.
• CPR certification required, ACLS preferred.

Responsibilities

• Conduct and coordinate daily clinical trial activities according to guidelines.
• Ensure medical well-being and safety of study participants.
• Evaluate and assess participants for eligibility.

Skills

Clinical skills including phlebotomy

Proficiency in MS Office and electronic health records

Strong organizational skills

Bilingual (English/Spanish)

Well-developed written and verbal communication skills

Education

MD or DO degree

Board certification in area of specialty

Job description

2 days ago Be among the first 25 applicants

Department: Operations

Location: North Georgia Clinical Research

Description: Alcanza is a growing multi‑site, multi‑phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, 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

• 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, and a minimum of 2 years of experience in a medical research environment, or an equivalent combination of education and experience, is required. Board certification in area of specialty preferred. CPR required / ACLS preferred.

Required Skills

• Clinical skills including phlebotomy, vitals, ECGs/EKGs, IVs, etc., and clinical procedures based on 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.

Seniority Level

Mid‑Senior level

Employment Type

Full‑time

Job Function

Research, Analyst, and Information Technology

Industries

Research Services

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