Medical Director, Cardiology

IQVIA LLC; Durham (NC); Remote; USD 155,000 - 432,000; Full time

Job summary

IQVIA is seeking a Medical Director specialized in Cardiology to provide medical, clinical and scientific advisory support across divisions. You will lead medical monitoring, review protocols and support BD activities on trials, with 24/7 availability for urgent protocol questions.

Qualifications include an MD/DO with board certification in Cardiology and 5–7 years in clinical medicine, plus clinical development experience and strong English communication skills.

Qualifications

• Medical degree from an accredited medical school.
• Board certification in Cardiology.
• 5–7 years of clinical medicine post residency.
• Clinical development experience (Ph I–IV) required.
• Pharma/CRO/biotech clinical research exposure.

Responsibilities

• Act as Global/Regional Medical Advisor on assigned projects.
• Provide medical monitoring and protocol/IDB/CSR support.
• Review SAEs and assist with pharmacovigilance activities.
• Deliver therapeutic area training to project teams.
• Attend investigator meetings and client discussions.
• Be available 24/7 for urgent protocol-related questions.

Skills

Medical expertise

Communication skills

Presentation skills

Interpersonal skills

English proficiency

Education

MD/DO medical degree

Board certification in Cardiology

Job description

Job Posting Title- Medical Director, Cardiology

Location: Home-based in the U.S.

Job Overview

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 as requested.

Essential Functions

The role includes predominantly Medical Monitoring responsibilities with therapeutic and medical expertise to Business Development activities as requested. Medical Monitoring: Primarily serves as Global and /or Regional 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.

Medical Strategy

Provides expert advice on the development of medically sounded delivery strategies for small to large and/or complex multi-region studies in partnership with sales and other functions responsible for business development activities. Responsible for the development of the medically related aspects of client proposals including the budget related to medical monitoring. Provides medical and scientific advice to key internal stakeholders developing proposals: this may include, but is not limited to, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Attend and present at bid defense preparation and bid defense meetings, as required. Participates in strategic business development activities including presentations to prospective clients. Maintains awareness of industry development and may author related publications. Requires periodic regional and international travel.

Qualifications

Board certification in Cardiology.

Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to the specific therapeutic area, plus a minimum of 5 years' experience in clinical medicine post residency period. Typically requires 5 - 7 years of prior relevant experience in the requested medical specialty area; In addition, previous clinical research experience as an investigator or in the Pharma, CRO, or Biotech industry is required. Experience in Clinical Development (Phase I -IV) Prior experience in cardiology with exposure to metabolic disease indications is preferred. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong communication, presentation and interpersonal skills, including good command of English language (both written and spoken). Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area. Proven skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. Current or prior license to practice medicine.

#LI-Remote #LI-NITINMAHAJAN

Company Information

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Compensation

The potential base pay range for this role, when annualized, is $154,900.00 - $431,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.