Senior Research Scientist, On-site, Wilmington, DE
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Job Location:
Wilmington, DE - USA
Monthly Salary:
$ 77100 - 160700
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Job Overview:
Candidate must be within commuting distance of Wilmington DE.
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.
Essential Functions:
- 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.
Qualifications
- Bachelors 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. 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.
The potential base pay range for this role when annualized is $77100.00 - $160700.00. 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.Required Experience:
Senior IC
Key Skills
- Laboratory Experience
- Machine Learning
- AI
- Bioinformatics
- Biochemistry
- Assays
- Research Experience
- Next Generation Sequencing
- Drug Discovery
- Research & Development
- Natural Language Processing
- Molecular Biology
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
