Job Title: Principal Clinical Data Manager
Salary: 120k-130k
Company Summary: Need an exciting career change? This role is for a mid-sized, full-service CRO that provides clinical research services within pharmaceutical, biotech, and medical device industries. The company has many locations across several states and countries and are looking to add to their award-winning teams. This role will be apart of the expansion of the Little Falls, NJ team with WFH and on-site options.
Responsibilities:
- Develop and maintain Data Management Project Plans, DQRP, Third-party non-CRF data management activities.
- Manage large volume of day-to-day activities for assigned projects
- Conduct training on EDC systems, Medidata RAVE and other processes related to dataflow, quality control, and clinical trial personnel.
- Design and review CRF's and eCRF's, clinical trial source document templates, and completion instructions.
Qualifications:
- Education: Bachelors/Masters in pharmaceutical sciences, physical/biological or chemistry fields.
- 5 year's experience in pharmaceutical clinical trial data management OR 2 years of CDM II experience.
- Knowledge of clinical trial data management concepts processes, pharmaceutical clinical trial regulations, conventions and standards.
- Strong leadership, driven attitude, ability to meet high standards.
Benefits:
- Fully remote
- Plenty of Growth opportunities
There are many positions open across several different levels, so feel free to apply to be considered for multiple vacancies! Apply directly to this job post and we will be in contact to set up a screening call!