Clinical Research Physician - Part-Time - 16-18 hours per week

Alcanza Clinical Research•Methuen, MA

7d•Onsite

About The Position

Alcanza is a growing multi-site, multi-phase clinical research company with locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX, and Puerto Rico. It conducts Phase I–IV studies in therapeutic areas including vaccines, neurology, dermatology, psychiatry, and general medicine. The Clinical Research Physician conducts and coordinates daily clinical trial activities in accordance with ICH/FDA/GCP guidelines, local regulations, study protocols, and company policies and processes. Working with local and central teams, the physician provides clinical oversight and supports the quality of assigned studies at the site. The position is part-time, scheduled for 16–18 hours per week, at ActivMed Practices & Research in Methuen, Massachusetts, and reports to Kathleen Valcich.

Requirements

MD or DO degree.
Active physician license in good standing in the state of practice.
Direct patient-facing experience.
Board certification in the area of specialty.
CPR certification required.
Clinical skills and clinical procedures in the physician’s area of specialty.
Proficiency with computer applications such as MS Office, electronic health records, and web applications.
Ability to type at least 40 words per minute.
Strong organizational skills, attention to detail, and math proficiency.
Well-developed written and verbal communication skills.
Well-developed interpersonal and listening skills, and ability to work effectively independently and with co-workers, employees, subjects, managers, and external customers.
Ability to handle multiple tasks and adapt to changes in workload and priorities.
Professionalism, respect for others, self-motivation, and a strong work ethic.
High degree of urgency, integrity, and dependability.
Ability to work independently to identify problems and implement solutions.
Ability to handle highly sensitive information confidentially and professionally in compliance with HIPAA guidelines.

Nice To Haves

ACLS certification.
English/Spanish bilingual proficiency.

Responsibilities

Ensure the medical well-being and safety of study participants through 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 support successful delivery and retention of study participants.
Interact positively and collaboratively with sponsors, clients, and team members.
Record data and participant information accurately and in accordance with protocol guidelines and GCPs.
Actively participate 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 participant, protocol, or company needs.