joblet.ai
Find JobsNearby JobsJobs for you
Sign inEmployers / Post a Job
joblet.ai

AI-powered job search connecting talent with opportunity.

ELEVEN AI, Inc.
200 Continental Drive, Suite 401
Newark, DE 19713

Product

  • Browse Jobs
  • Job Locations
  • Browse by Companies
  • Post a Job
  • Blog
  • FAQ
  • Jobs Near Me

Company

  • About Us
  • Contact
  • Refer & Earn
  • Explore all pages

Legal

  • Privacy Policy
  • Cookie Policy
  • Terms of Service

Browse jobs by industry

  • AI
  • IT Services
  • Healthcare
  • Manufacturing & Production
  • Supply Chain
  • Infrastructure
  • Transport & Logistics
  • Real Estate
  • Finance & Accounting
  • Consulting
  • Sales & Marketing
  • Hospitality
  • Media & Entertainment
  • Education

© 2026 ELEVEN AI, Inc. joblet.ai is a product of ELEVEN AI, Inc. All rights reserved.

Overview

Company
Avery Healthcare Group
Location
all cities, CA 5
Employment type
On-site
  • FACS (Family Consumer Sciences) Gr 6-8 Teacher, 0.2 FTE (5)
  • Lead EIT Engineer (FPSO E-House, offshore/onshore Marine) (5)
  • Senior SecOps Automation Engineer - Consumer FinTech | Colombia (5)
  • Remote VAC/Water Truck Driver -Prudhoe Bay (42)
  • Drafter - Remote (38)
  • Opto-Mechanical - REMOTE (51)
Back to Jobs
Avery Healthcare GroupVerified Employer

Business Services & Consulting • all cities, CA 5

Associate Medical Director- Oncology ,Sponsor-Dedicated (12 months Fixed Term Contract) (5)

all cities, CA 5On-sitePosted 1 day ago
Business Services & Consulting

About the Role

Associate Medical Director / Medical Director

The Associate Medical Director / Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities.

Essential Functions
  • Primarily serves as Global Medical Advisor on assigned projects.
  • Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects.
  • Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
  • Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
  • Provides therapeutic area/indication training for the project clinical team.
  • Attends and presents at Investigator Meetings.
  • Performs review and clarification of trial-related Adverse Events (AEs).
  • May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.
  • May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.
  • May perform medical review of adverse event coding.
  • Performs review of the Clinical Study Report (CSR) and patient narratives.
  • Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
  • Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws.
  • May require regular travel.
  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
Qualifications
  • Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
  • 5-7 years of experience in clinical medicine
  • Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
  • Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
  • Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
  • Excellent oral and written communications skills as well as interpersonal skills are essential.
  • Board certification or board qualifications in medical oncology, radiation oncology, hematology or internal medicine (with hematology or oncology experience)
Associate Medical Director / Medical Director

The Associate Medical Director / Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities.

Essential Functions
  • Primarily serves as Global Medical Advisor on assigned projects.
  • Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects.
  • Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
  • Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
  • Provides therapeutic area/indication training for the project clinical team.
  • Attends and presents at Investigator Meetings.
  • Performs review and clarification of trial-related Adverse Events (AEs).
  • May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.
  • May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.
  • May perform medical review of adverse event coding.
  • Performs review of the Clinical Study Report (CSR) and patient narratives.
  • Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
  • Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws.
  • May require regular travel.
  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
Qualifications
  • Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
  • 5-7 years of experience in clinical medicine
  • Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
  • Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
  • Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
  • Excellent oral and written communications skills as well as interpersonal skills are essential.
  • Board certification or board qualifications in medical oncology, radiation oncology, hematology or internal medicine (with hematology or oncology experience)

What You'll Do

Primarily serves as Global Medical Advisor on assigned projects.
Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects.
Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
Provides therapeutic area/indication training for the project clinical team.
Attends and presents at Investigator Meetings.

Skills & Technologies

Business Services & Consulting

Similar jobs

FACS (Family Consumer Sciences) Gr 6-8 Teacher, 0.2 FTE (5)
Minnesota Service Cooperatives
all cities, CA 5Posted 10 days ago
Lead EIT Engineer (FPSO E-House, offshore/onshore Marine) (5)
GE Vernova
all cities, CA 5Posted 7 days ago
Senior SecOps Automation Engineer - Consumer FinTech | Colombia (5)
TrueLogic Company
all cities, CA 5Posted 19 hours ago
Remote VAC/Water Truck Driver -Prudhoe Bay (42)
NANA Management Services
all cities, SD 42Posted 11 days ago
Drafter - Remote (38)
Katmai Government Services
all cities, OR 38Posted 11 days ago
Opto-Mechanical - REMOTE (51)
KBR
all cities, WY 51Posted 19 hours ago
Avery Healthcare Group
Business Services & Consulting
View all jobs at Avery Healthcare Group