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Senior Clinical Data Management Consultant
1 month ago
We are seeking a Senior Clinical Data Management Consultant to join our team at Veeva Systems, Inc. in the United States.
About the RoleThis is a challenging and rewarding opportunity for an experienced consultant with expertise in clinical data management to work with life sciences companies and help them optimize their use of EDC in running clinical trials.
You will be responsible for understanding customers' data management needs and challenges, offering guidance and direction to ensure that the clinical trial is designed with deliverables in mind.
As a key member of our CDMS Professional Services team, you will be at the forefront of our mission and responsible for four main things:
- Understanding customers' data management needs and challenges, offer guidance and direction to ensure that the clinical trial is designed with deliverables in mind.
- Ensuring that the CDMS application adheres to Good Clinical Data Management Practices and Veeva standards to optimize value.
- Responsible for authoring all specification documents used by team members and configuring the study design during the development phase of the project inclusive of forms, rules, and study configuration.
- Supporting developers and testers during the project lifecycle.
You will be part of a talented team of consultants who are passionate about delivering high-quality services to our clients.
Our team is committed to helping life sciences companies bring therapies to patients faster, and we are looking for someone who shares our vision and values.
RequirementsTo be successful in this role, you will need to have:
- 2+ years' experience in end-to-end data management-related activities (database design, data collection, data analysis, query resolution, datasets, statistical reporting).
- 2+ years' direct experience working with EDC clinical software solutions in clinical operations and/or trial management in a project management/consultant role.
- Life sciences industry experience and knowledge of clinical trial process preferred (pharmaceutical, biotech, medical device companies, CRO's, and academic & public health organizations).
- Experience in a customer-facing role, preferably with a software professional services organization or consulting background, is preferred.
- Working Knowledge of Clinical Trial processes across pharmaceuticals, device, and/or biotech sectors, specifically as they relate to design, document, and data collection.
- Ability to quickly understand business requirements.
- Proven ability to work independently in a dynamic environment but also as part of a team.
- Logical approach to problem solving.
- Ability to manage multiple tasks and project deliverables.
- Proven track record of meeting project timelines/deliverables and attention to detail, process, deadlines, and quality results.
- Demonstrated success with customers during project assessment, planning, development, training, and implementation.
- Excellent verbal and written communication, interpersonal, and presentation skills.
- Ability to travel 20-25% (may include international).
As a Senior Clinical Data Management Consultant at Veeva Systems, Inc., you can expect a competitive salary of $120,000 per year, plus benefits including health insurance, retirement plan, and paid time off.
We also offer a generous budget for training and development, as well as opportunities for career growth and advancement.
LocationThe ideal candidate will be based in the San Francisco Bay Area, with opportunities to work from home or in our offices in more than 15 countries around the world.
