Celebrating 40+ years!

Theradex Oncology is a full-service CRO specializing in oncology. The company manages global oncology trials and programs. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics. As a service-based company we support both domestic and international sponsors in the conduct of both early and late phase trials.

Remote-US Preference will be given to candidates located in the tri-state area (commutable to Princeton, NJ)

As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference.

Opportunity

Clinical Data Manager/Sr Clinical Data Manager - dependent upon experience

You will play a pivotal role in ensuring the integrity and quality of our clinical trial data. You will collaborate closely with cross-functional teams and manage data management activities for multiple studies.

The primary responsibilities of this position include, but are not limited to, the following:

• Perform all clinical data management activities in compliance with SOPs and ICH-GCP regulatory requirements
• Work closely and collaboratively with the SAS Programming team, biostatistics team and other data managers
• Act as lead clinical data manager on multiple studies of moderate complexity with minimal supervision
• Serves as the main point of contact for study DM related matters
• Lead DM Study Start-Up Activities
• Conduct EDC User Acceptance Testing and program validations.
• Develop programs in SAS/EXCEL for study data metrics monitoring and clinical data review.
• Perform comprehensive data review of all patient data.
• Perform WHO Drug Dictionary coding and MedDRA coding as necessary
• Support Project Team through:
  • Tracking and provision of project status updates to project managers for monthly project team meetings
  • Close communication with CRA's to identify and mitigate negative data trends/issues
  • Provision of listings/reports as needed
  • Create ad-hoc reports for special data requests from Sponsor
  • Ensure that documentation is maintained in a state of constant audit-readiness and filed in the Trial Master File.
  • Coordinate all activities in preparation for study milestones and database lock
• May assist in the mentoring of less experienced employees
• Manage and prioritize project deliverables per established study timelines

Level of Education and Prior Experience

• Bachelor's degree required / Master's degree preferred
• 3-5 Years relevant data management experience in the CRO / pharmaceutical industry required
• EDC experience required, RAVE EDC experience preferred
• SQL/SAS programming experience preferred

Skills and Competencies

• Demonstrates knowledge of GCPs and protocol
• Strong understanding of CDISC CDASH and SDTM Standards
• Highly effective ability to anticipate problems relating to projects and to develop and implement solutions
• Excellent interpersonal skills
• Fluent knowledge of written and verbal English
• Highly organized and result-oriented
• Strong communication, comprehension and logic skills
• Ability to work independently with minimal supervision as well as in a team environment
• Proficient in Word and Excel
• Ability to understand high level programming languages
• Strong time management and prioritization skills to meet deadlines among multiple projects

What We Offer

At Theradex we offer a supportive culture that puts people first. Our employees are eligible to participate in our comprehensive benefits package which includes medical, dental and vision coverage; life insurance, disability insurance (STD/LTD), company matched 401(k), competitive tuition reimbursement, generous vacation/sick plans, flexible work schedules, employee discounts and other company provided benefits. The annual base salary for this position ranges from $80,000-$145,000 with bonus potential. We will assess the specific title and level of entry during the interview and assessment process since the actual salary offer will be based on a number of factors, including but not limited to the candidate's qualifications, experience, skills, and competencies for the role.

This position is not eligible for relocation or company provided sponsorship.