Senior Research Scientist

Job Overview

Provide medical, clinical and scientific advisory expertise to all departments as requested. Participate in all aspects of Medical Science involvement on assigned trials. Perform work in accordance with ICH E6 Guideline for Good Clinical Practice.

• Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements.

• Review and evaluate clinical data in the generation of study concepts and protocols in the relevant therapeutic area and maintaining a high level of awareness of scientific developments and the competitive environment to assist on ongoing strategic re-evaluation of the program.

• Work closely with the Clinical Operations, Clinical Sciences and Global functional teams to ensure the translation of the protocol and clinical development plans into executable operational processes.

• Lead internal or external training as required and support the medical monitor in responses to investigators and other site personnel regarding clinical and study conduct questions.

• Independently review study subject level data for presentation to the medical monitor for clinical decision making, throughout the study life cycle. Liaises closely with the clinical safety scientist to support ongoing aggregate safety data review during a given clinical study.

• May manage alone or in collaboration with clinical safety the operational functioning of data monitoring committees and/or clinical adjudication committees. Clinical Scientist may participate in and present at these meetings, as required.

• Participate in analyzing and interpreting data from clinical studies, and writing/editing or reviewing results in study reports, regulatory submissions, abstracts, posters, presentations, peer reviewed manuscripts, and other documents. As required, lead internal data review meetings to determine strategic interpretation.

• May become a member of the company publication group. Additionally serve as a scientific reviewer for company publications and external research proposals in the area(s) of expertise.

• Participate in the Clinical Operations and Clinical Development teams. Provide support to the clinical development team (CDT) through meeting management support and communication. Act as the delegate or lead where required.

• Interact with internal auditing groups on a study level to ensure clinical development activities are conducted according to internal SOPs and work practices and in compliance with ICH-GCP.

• Bachelor's Degree or equivalent experience

• 3-5 Years of relevant industry experience

• Excellent communication (interpersonal, verbal and written) skills, ability to communicate effectively at all levels.

• Knowledge of PC applications

• Ability to work with global teams

• Ability to travel

• Knowledge of Health/Safety and Environment good practice.

• Duty to comply with all applicable standards as required by the company

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

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.

The potential base pay range for this role, when annualized, is $77,100.00 - $. 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.

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