Senior Data Manager, Lead Data Manager

Senior Data Manager, Lead Data Manager at Lifelancer in United States.

Role Summary

• Job Title: Senior Data Manager, Lead Data Manager
• Job Location: Kirkland, Quebec, Canada
• Job Location Type: Remote
• Job Contract Type: Full-time

Requirements

Practical experience

• Design of electronic CRFs
• Developing Editing Controls
• Query management
• Managing database locks
• Data reconciliation process
• Experience managing SDTM datasets and clinical data transfers.
• Good understanding of CDISC and CDASH standards, as well as regulatory requirements.
• Minimum 7+ years of Clinical Data Management experience in pharmaceutical, biotechnology, or CRO environments.
• Strong knowledge of clinical trial processes from study start-ups through closeout.
• Experience leading Data Management activities for global clinical trials.
• Experience managing high-complexity studies, preferably in Oncology.

Hands-on experience with

• eCRF design
• Edit check development
• Query management
• Database lock activities
• Data reconciliation processes
• Experience with SDTM dataset management and clinical data transfers.
• Strong understanding of CDISC, CDASH, and regulatory requirements.

IQVIA is a leading global provider of clinical research, business information and healthcare intelligence services to the life sciences and healthcare industries. IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. To learn more, visit

IQVIA is proud to be an employer subscribing to the principle of equal access to employment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status or any other status protected by applicable law. Accommodations for applicants with disabilities are available upon request in all aspects of the recruitment process. If you have a disability that requires an accommodation, we encourage you to contact our talent acquisition team at , so that IQVIA can support your participation in the recruitment process.

IQVIA is committed to integrity in its recruitment process and has a zero tolerance policy on candidate fraud. All information and qualifications submitted in your application must be true and complete. Any misrepresentation, misleading presentation or material omission during the recruitment process will result in immediate disqualification of your application, or termination of employment if later discovered, in accordance with applicable laws. We appreciate your honesty and professionalism.

Please note that we may use artificial intelligence (AI) in processing your application. However, we use AI only to help our recruiting team screen or evaluate candidates, and not to replace decision-making by our team members.

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, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: , so that IQVIA can support your participation in the recruitment process.

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.

Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidates, and not as a substitute for human decision-making.

The potential base salary range for this position, annualized, is $108,300.00 - $144,452.88. The actual base salary offered may vary depending on several factors, including job-related qualifications such as knowledge, skills, training and experience; location; and/or schedule (full-time or part-time). Depending on the position offered, incentive plans, bonuses and/or other forms of compensation may be offered, in addition to a range of health, wellness and/or other benefits. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; rental; 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 wellness and/or other benefits.

• This job is curated by Lifelancer.
• Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
• Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
• At least 7 years of experience in clinical data management in the pharmaceutical, biotechnology sectors or within a CRO.
• Strong knowledge of clinical trial processes from initiation to closeout.
• Experience in data management for international clinical trials.
• Experience managing complex studies, preferably in oncology.