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Mgr, Data Reporting

  • Cambridge, Massachusetts, United States
  • Full Time

About the Job

The Manager, Data Reporting oversees medical reporting for FMI’s  pharmaceutical and academic research partners  and directly supervises the  Data Reporting team. This role serves as a key liaison between Clinical Operations, Data Operations and FMI Information Technology teams. 

Key Responsibilities

• Lead the Data Reporting team and direct work allocation, project oversight, task assignments, and prioritization.

• Manage and develop direct reports, supporting ongoing professional development and growth, and perform applicable evaluation, hiring, and day-to-day management.

• Manage review and approval of new data reporting specifications for our research  partnerships.

• Manage daily reporting requirements.

• Act as key internal point of contact for internal Information Technology teams to propose, prioritize, test, and implement improvements to  internal data reporting applications.

• Support team messaging with respect to technology updates.

• Support team messaging with respect to corporate updates.

• Develop scalable solutions to enhance data reporting processes.

• Support development and maintenance of Data Operations Standard Operating Procedures and work instructions.

• Assist with prioritization of data reporting deliverables and technology requests.

• Provide point of escalation support to team.

• Other projects as assigned.

Qualifications

Basic Qualifications

• Bachelor’s Degree in a scientific or related field

• 5+ years of professional data management or project management experience in an academic, life sciences, or Contract Research Organization (CRO) environment involving management of clinical data

• 2+ years of work experience managing or leading a team

Preferred Qualifications

• 7+ years of professional experience in scientific data management in all phases of project design and analysis

• Excellent communication skills, including ability to diffuse difficult conversations

• Knowledge of and experience working within Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and other regulatory standards

• Proven ability to manage projects and/or resources

• Experience with multi-disciplinary scientific data management approaches, including project planning, user training, managing audit of transfers by external stakeholders

• Familiarity with oncology, molecular biology, genetics, and/or bioinformatics

• Understanding of HIPAA and the importance of patient data privacy

• Demonstrated ability to:

·   Quickly learn new software/technology

·   Collaborate with peer groups in a way that facilitates strategic and tactical planning for excellent interaction with outside collaborators and clients

·   Perform assignments with minimal supervision

·   Work well under pressure while maintaining a professional demeanor

·   Prioritize and thoroughly follow up on assigned tasks

·   Handle multiple tasks at once and work in a fast-paced environment

·   Adapt to changing procedures, policies and work environment

• Demonstrated integrity

• Commitment to values held at FMI: patients, innovation, collaboration, and passion

Apply Now

Internal applicants, please use your FMI email address.

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