Associate Data Manager

Posted 14 Days Ago
Be an Early Applicant
Budapest
1-3 Years Experience
Healthtech • Software
The Role
Clario is seeking Associate Data Managers to ensure data quality and reporting for sponsors. Responsibilities include quality checks, communication with teams, documentation, client reconciliation, and process improvement. Requires BS/BA in Life Sciences, 2 years of clinical research/data experience, familiarity with clinical data reports, GCP, and strong organizational skills. Knowledge of SAS, SQL, and CDISC SDTM is a plus.
Summary Generated by Built In

Clario is seeking talented Associate Data Managers and Data Managers to ensure the highest quality of data processing and reporting for our Sponsors. Located in our Budapest office, you will be the primary contact for all data-related issues, defining the methods and tools used by Clario to deliver exceptional services. If you have a passion for data integrity and enjoy collaborating with both internal and external teams, we invite you to be a part of our innovative and dynamic team.

What we offer

  • Competitive compensation

  • Attractive benefits (security, flexibility, support and well-being)

  • Engaging employee programs

  • Flexible hybrid working model

  • OTP Szép Card

What you'll be doing

  • Perform quality and/or consistency checks on the output file(s) generated by study specific programs where required. This can include comparing individual data points of the final output data to the corresponding data points of the original dataset based upon the gathered requirements and/or edit check output.

  • Communicate with appropriate Clario staff (i.e. Data Manager, Science teams, medical staff) regarding any discrepancies found and document all results and/or changes.

  • Work on study documentation (DMP/DTS) under the guidance of the 

  • Data Manager and also assist in getting study documentation prepared for client review.

  • Serve as a point of contact for updates needed to the CDM task schedule (i.e. edit checks, transfer scheduling, Final data transfer checklist, etc.) and ensure they are being completed and/or maintained.

  • Assist with metrics related to data issues or file delivery as well as ensuring the systems have correct information regarding study assignment.

  • Provide assistance to CDM team for documents, presentations, etc. that require template updates and formatting changes.

  • Serve as primary recipient of client reconciliation feedback between data transfers and ensure appropriate investigation and/or action on those requests within the agreed turnaround time.

  • Ensure good quality documentation is maintained in regard to the client reconciliation feedback.

  • Communicate project status clearly with Clients and Project Management.

  • Assist with the maintenance and storage of study documentation relative to data management activities.

  • Contribute to continuous process improvement including workflow efficiencies and associated workflow documentation.

  • Assist in CAPA issues related to study-specific data management activities.

What we look for

  • BS/BA Degree in Life Sciences or related field

  • Minimum of 2 years experience working with clinical research/data

  • Familiarity with clinical data reports, GCP, and general understanding of clinical trials

  • Strong organizational, interpersonal, analytical and communication skills

  • Detail-oriented

  • Experience with Windows and Microsoft Office products preferred

  • Ability to communicate effectively in English 

  • SAS and/or SQL exposure or experience a plus

  • Knowledge of CDISC SDTM is a plus

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

Top Skills

SAS
SQL
The Company
HQ: Philadelphia, PA
6,733 Employees
On-site Workplace
Year Founded: 1972

What We Do

-- Clario has been named a Top Workplace by Energage for the 2022 Top Workplaces USA national awards. --

Clario generates the richest clinical evidence by fusing our deep scientific expertise and global scale into the broadest endpoint technology platform. By doing this, we empower our partners to transform lives.

With almost 50 years of experience, 19,000 clinical trials, and 870 regulatory approvals, Clario has mastered the ability to generate rich evidence across a Trial Anywhere™ portfolio: decentralized (DCT), hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe, and Asia Pacific, Clario delivers the power of certainty.

Partners
—————
Clario brings the best of ERT and Bioclinica together to
work alongside our partners to solve some of their biggest questions on topics such as:
- eCOA vs. paper
- Decentralized Clinical Trial (DCT)
- Rescue a clinical trial
- Broad endpoint technology: cardiac safety, imaging, respiratory

And many more.

People
————
We are so honoured to be named a 2022 Top Workplace by Energage. One of our leading values at Clario is People First Always. We help individuals build meaningful careers at Clario as they serve to help transform patients lives.

Join us on this journey and check out our careers page:

https://clario.com/careers/

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