Medical Director- Neurology at IQVIA

Belgrade, Serbia

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Clinical Research, HealthcareIndustries

Requirements

Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education
Minimum of 5 years' experience in clinical medicine
Specialty board certification
Ideally, minimum 2 years clinical trials experience as an investigator or medical/clinical expert in the Pharma, CRO, or Biotech industry
Ability to establish and maintain effective working relationships with co-workers, 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, as well as initiative and flexibility

Responsibilities

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
Primarily serve as Global and/or Regional Medical Advisor on assigned projects
Serve as Scientific Advisor and provide guidance to Project Leaders on the medical and scientific aspects of assigned projects
Provide 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
Perform medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs)
Provide therapeutic area/indication training for the project clinical team
Attend and present at Investigator Meetings
Perform 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
Perform review of the Clinical Study Report (CSR) and patient narratives
Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested
Available 24/7 to respond to urgent protocol-related questions from investigative sites, in accordance with local labor laws
Provide expert advice to the development of medically sound 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
Provide medical and scientific advice to key internal stakeholders developing proposals, including 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 meetings, as required
Participate in strategic business development activities including presentations to prospective clients
Maintain awareness of industry developments and may author related publications
Requires periodic regional and international travel

Skills

Neurology

Medical Monitoring

Pharmacovigilance

Clinical Trials

Protocol Review

Adverse Events

Serious Adverse Events

Clinical Study Report

Investigator Meetings

Medical Strategy

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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