Clinical Site Lead Job at GForce Life Sciences, Los Angeles, CA

QVNVa1VicWlJL29PTTQycVRML0RKcWkzclE9PQ==
  • GForce Life Sciences
  • Los Angeles, CA

Job Description

Summary

Our client, a Fortune 500 Medical Device company, has engaged GForce Life Sciences to source a skilled Clinical Site Lead (CSL). The CSL will oversee clinical study site maintenance, data collection, and field monitoring to ensure compliance with protocols, regulations, and Good Clinical Practices. Responsibilities include managing essential documents, resolving data discrepancies, reviewing adverse events, and coordinating site initiation. The role requires analytical problem-solving, process optimization, and continuous quality improvement. The CSL will monitor site performance, identify areas for improvement, and provide solutions to management.

Job Duties

  • Monitors clinical studies at sites in an assigned territory (and others as requested) to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of site initiation, periodic, and close-out visits.
  • Ensures both regulatory and clinical protocol compliance is maintained for all assigned clinical projects.
  • Reviewing data and source documentation from investigational sites for accuracy and completeness
  • Ensuring adverse events and protocol deviations are reported in an efficient manner
  • Ensuring that device complaints and malfunctions are reported according to the client’s Policies and Procedures
  • Resolving and/or facilitating resolution of problems including identification of cause and actions to prevent reoccurrence
  • Coordinates with study teams, field clinical engineers or designee and specialists.
  • Enroll sites into new and ongoing clinical studies
  • Facilitate enrollment of study subjects via site coordinators
  • Facilitate resolution of data queries and action items at clinical sites
  • Promptly reports the findings of monitoring visits according to the client’s processes.
  • Collaborates with in-house teams to ensure complete submission of study documents.
  • Trains site personnel to ensure compliance with the study protocol and local regulations.

Requirements

  • Bachelor’s Degree - Preferably with an academic focus in natural science, pre-medicine, nursing, bioengineering, or a related academic field.
  • 10+ years of clinical trial monitoring experience required.
  • Familiarity with cardiac, vascular, and/or neuromodulation technologies.
  • Previous related experience in a medical device/pharmaceutical company or relevant clinical experience in a clinical/hospital environment.

Preferred Qualifications

  • A general familiarity with cardiac, vascular, and/or neuromodulation technologies.
  • Certification by an industry-recognized professional society (i.e. Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) or accredited institution

Term & Start

  • Remote with travel to sites in SoCal
  • 50-75% travel (depending on clinical trials)
  • 12-month contract (extension probable)
  • Benefits available (Medical, Dental, Vision, 401k)

Job Tags

Contract work, Local area, Remote work

Similar Jobs

Access Infusion Care Inc

Nurse Practitioner (NP) or Physician Assistant (PA-C) Job at Access Infusion Care Inc

 ...compassionate, and team-oriented full-time Nurse Practitioner (NP) or Physician Assistant (PA-C) to join our growing Internal Medicine Specialty/...  ...outpatient environment focused on high-quality patient care, chronic disease management, biologic therapies, and long-term... 

Carnegie Mellon University

Postdoctoral Research Associate Job at Carnegie Mellon University

 ...scale DNA samples. Our work has been published in venues like SenSys, MobiSys, CHI, UIST, IROS, and Nature-family journals (Communications, Biomedical Engineering, Digital Medicine). Pittsburgh is a great city, CMU is an amazing place to do research, and the... 

Applebee's

Host / Hostess Job at Applebee's

 ...experiences to our Neighborhood Guests and a place to belong for our Team Members. We're looking for Full Time & Part Time: HOSTS / HOSTESSES Requirements: Must be 18 years of age, or older Previous restaurant / teamwork oriented experience preferred, but we can... 

Global Connect Technologies

Embedded UI developer Job at Global Connect Technologies

 ...Experience with UI development for embedded products using web browser-based technologies ( javascript, etc) Experience with...  ...functional stakeholders for product requirements Experience developing embedded software for measurement and analytical equipment developed... 

Eataly North America

Cooking Class Host Job at Eataly North America

 ...Events Manager. Warmly welcome guests attending consumer and private events at La Scuola. Support the Chef during scheduled classes and events by anticipating their needs and that of the La Scuola guests. Setup dining area with the proper floorplan silverware...