Lead Clinical Investigator – Phase I-IV Trials

ActivMed Practices & Research, LLC.

Methuen (MA)

Vor Ort

USD 180.000 - 240.000

Vollzeit

Vor 10 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability insurance
HSA
401k plan

Zusammenfassung

Alcanza Clinical Research is hiring a Principal Investigator to oversee clinical trials across multiple sites. You will lead daily trial activities, ensure patient safety, and drive protocol compliance under ICH/GCP guidelines and HIPAA regulations.

Ideal candidates hold an MD/DO with an active license, board certification, and CPR/ACLS as needed. You will coordinate with sponsors, manage recruitment, and ensure high-quality data across studies.

Qualifikationen

  • MD or DO degree with active state license.
  • Board certification in specialty required.
  • CPR required; ACLS preferred.

Aufgaben

  • Lead site operations ensuring patient safety and protocol compliance.
  • Coordinate daily clinical trial activities per ICH/FDA/GCP and HIPAA.
  • Oversee participant recruitment, enrollment, and retention.
  • Collaborate with sponsors, clients and team members.
  • Maintain accurate data entry and documentation per protocol.

Kenntnisse

Clinical skills
MS Office
EHR proficiency
Typing 40 wpm
Bilingual EN/ES
Organizational skills
Attention to detail
HIPAA compliance
Independent worker

Ausbildung

MD/DO degree
Board certification
Active medical license

Tools

MS Office Suite
Electronic Health Records

Jobbeschreibung

Alcanza Clinical Research is hiring a Principal Investigator to oversee clinical trials across multiple sites. You will lead daily trial activities, ensure patient safety, and drive protocol compliance under ICH/GCP guidelines and HIPAA regulations.

Ideal candidates hold an MD/DO with an active license, board certification, and CPR/ACLS as needed. You will coordinate with sponsors, manage recruitment, and ensure high-quality data across studies.

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