Icon hamburger
Briefcase

Create Job Alert.

Enter your email below to save this search and receive job recommendations for similar positions.
Thank you. We'll send jobs matching these to
You already suscribed to this job alert.
No Thanks
US
What job do you want?

Create Job Alert.

Get similar jobs sent to your email

Apply to this job.
Think you're the perfect candidate?
Apply Now
Thumsup

You’re being taken to an external site to apply.

Enter your email below to receive job recommendations for similar positions.
Sr. Clinical Data Manager at

Sr. Clinical Data Manager

Cambridge, massachusetts, MA Contractor
Apply Now

Create Job Alert.

Get similar jobs sent to your email

Sr. Clinical Data Manager

6 month extendable

Cambridge, MA

307671


Must be able to sit onsite after stay at home.  3 years sponsor company experience preferred. Oncology clinical trial TA preferred.


Job Description

  • Provides support to Legacy studies 
  • Manages data activities for all clinical trials 
  • Designs case report forms (CRFs) as well as data edit checks and aggregate check specifications with CROs.
  • Works in coordination with statisticians and programmer/analysts.
  • Works in coordination with clinical research and development, clinical operations, and CROs 
  • Primary interface with CROs for any data management related activities.
  • Ensures that data management tasks remain on target according to study timelines and requirements.
  • Proactively works with CROs to organize on-going data review throughout the study to ensure timely identification and correction of errors or discrepancies.
  • Routinely communicates site data concerns/issues with clinical operations team and CROs in order to ensure collaboration toward resolution.
  • Ensures delivery of a quality locked database for analysis at the close of studies.
  •  
  • Education: Bachelor’s degree or equivalent combination of education/experience in math, science or health-related field.

    • Minimum of 3-5 years of clinical trial data management experience in the biopharma industry
    • Strong understanding of clinical trial process and EDC platforms.
    • Experience with data programming tools and/or data viewing tools (J-Review, SAS JMP.etc).
    • Excellent communication and organizational skills, along with problem solving, conflict resolution, leadership and team-building skills.

Recommended skills

Clinical Research
Clinical Trials
Coherent Remote File System (Crfs)
Coordinating
Case Report Forms
Leadership
Apply to this job.
Think you're the perfect candidate?
Apply Now

Help us improve Careerbuilder by providing feedback about this job: Report this job

Report this Job

Once a job has been reported, we will investigate it further. If you require a response, submit your question or concern to our Trust and Site Security Team

Job ID: 307671

Careerbuilder TIP

For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.

By applying to a job using Careerbuilder you are agreeing to comply with and be subject to the Careerbuilder Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.