Associate Data Manager (Medical Imaging)

 

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Are you seeking a purposeful and rewarding career in Clinical Data Management?

Our eCOA, Cardiac Safety, Medical Imaging, and Respiratory operations are growing, and with big ambitions and a clear vision for the future, now is the time to join Clario’s industry leading Medical Imaging Data Management team.

What we offer

• Highly Competitive compensation
• Attractive benefits package (Healthcare, Pension, Support & well-being, & more)
• Remote & flexible working
• Engaging employee programs
• In-depth company & role specific onboarding programs
• OTP Szép Card (Hungary specific)
• Excellent learning & development opportunities

What you’ll be doing:

The Associate Data Manager works as part of our Medical Imaging Project Teams and plays an integral part in ensuring that rich, high quality data is obtained, processed, and reported to Sponsors throughout assigned studies. You will work within an overall project team, collaborating to deliver complex projects & contributing throughout the entire project lifecycle from initial set-up to project close & database lock. Responsibilities within this position will include (but may not be limited to):

• Performing 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.
• Communicating with appropriate Clario staff (i.e. Data Manager, Science teams, medical staff) regarding any discrepancies found and document all results and/or changes.
• Working on study documentation (DMP/DTS) under the guidance of the Data Manager and assisting in preparing study documentation for client review.
• Serving 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.
• Serving as primary recipient of client reconciliation feedback between data transfers and ensuring appropriate investigation and/or action on those requests within the agreed turnaround time.
• Ensuring good quality documentation is maintained in regard to the client reconciliation feedback.
• Communicating project status clearly with clients and project teams
• Assisting with the maintenance and storage of study documentation relative to data management activities.
• Contributing to continuous process improvement including workflow efficiencies and associated workflow documentation.
• Assisting in investigating CAPA issues related to study-specific data management activities.
• Assisting with metrics related to data issues or file delivery as well as ensuring the systems have correct information regarding study assignment.

What we look for:

• BSc, MSc, PhD in a relevant subject related to the Pharmaceutical / Healthcare / Life Science industry is preferred
• Demonstrable experience working within the Life Science / Pharma/Biotech / Clinical Research industry and a good basic understanding of the role that Data Management plays within Clinical Trials
• Ability to understand and interpret clinical trial documentation & protocols
• Experience working in compliance with FDA/EMA & GCP regulations
• Previous experience working with Medical Imaging, eCOA, IRT/RTSM, eConsent, ePRO or other eClinical / Clinical technology solutions is highly advantageous to applicants
• A background in Clinical Research, working as a Clinical Research Associate (CRA), Study coordinator, Project Assistant, Project Coordinator or similar positions is highly advantageous to applicants
• Previous SAS or SQL exposure or experience is advantageous to applicants
• Knowledge of CDISC / STDM is advantageous to applicants.

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. #LI-DNI

The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. Clario reserves the right to amend or change this job description to meet the needs of Clario.

This job description and any attachments do not constitute or represent a contract. The Department Head has the discretion to hire personnel with a combination of experience and education, which may vary from the above-listed qualifications.

Courageously Curious

Our appetite to blend the best of domain expertise, technology and human understanding knows no bounds. We’re relentless in pursuing the information, insights and inspiration that means we can continuously improve clinical trial site support services and technology solutions.

Behaviors:

• We learn; embracing change, questioning how we work, finding a better way. And if it doesn't go to plan, we don't blame each other; instead, we own it and grow together
• We partner' with each other, with customers, patients and sites, working with them to understand their goals and then deliver the best solutions, Deliver Exceptional

We step forward because responsibility powers us; we don’t leave others to do what we can do ourselves. We take charge of events, delivering exceptional work for our customers, patients and each other.

Behaviors:

• We prioritize; focusing on what matters, never compromising on quality.
• We commit; delivering what we say we will, working with energy and intent, sharing what we learn with each other., People first, always

We think of others before we think of ourselves. We have a deep understanding of our customers, and deep empathy for patients—and each other. We’re united by our purpose—it’s why we go above and beyond to support each other, emphatically.

Behaviors:

• We do the right thing; for our customers, patients, sites and each other. And We're passionate about it.
• We lift each other up; respectful of different views, we listen are inclusive, and support each other to succeed.

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