Clinical Data Manager Project Manager

Role Description

Join Us as a Clinical Data Manager Project Manager – Make an Impact at the Forefront of Innovation. As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Clinical Data Manager Project Manager, you will act as a study manager for multiple studies individually or as a program of several studies. You may perform the Project Manager role for standalone studies. Your responsibilities will include functional, administrative, and financial oversight of assigned projects.

• Provide support and coaching to the DM team to ensure that all tasks are completed accurately, on time and within budget to meet or exceed client expectations.
• Act as a primary liaison for project team and client.
• May develop and implement study specific training for DM project staff and performs independent reviews of DM deliverables following CDM guidelines.
• Monitor, evaluate and propose mitigation strategies surrounding risk to deliverables and finances.
• Participate in business development activities by assisting with bid preparation and representing data management at bid defense meetings, where required.
• Promote repeat business by developing relationships with new and existing clients.
• Perform project forecasting of hours and identification of resource requirements and manage project budgets including identification of out of scope work and participate in the Contract Modification process.
• Participate in the development and implementation of processes, procedures and training for the data management function as directed.
• Mentor junior level staff and peers on all associated tasks within a study or program.
• Independently lead and delegate tasks to ensure timely completion of project activities to project timelines, quality and budget.

Qualifications

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification.
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).
• In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Requirements

• Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations.
• Ability to use interactive computer programs.
• Excellent written/verbal communication skills with a strong command of English language and grammar.
• Strong organizational and analytical/problem solving skills; strong customer focus and excellent interpersonal skills.
• Ability to identify project risks and to effectively evaluate and develop plans to mitigate those risks.
• Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data.
• Ability to act as a study or department expert for DM processes.
• Ability to train and direct a study team, providing leadership and direction to both subordinates and peers.
• Ability to forecast project resourcing, project timeline planning and adherence to timelines.
• Ability to supervise and delegate tasks.
• Ability to successfully apply above skills, knowledge and abilities across a portfolio of studies.

Working Conditions and Environment

• Work is performed in an office environment with exposure to electrical office equipment.
• Occasional drives to site locations with occasional travel both domestic and international.

Benefits

• When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence.
• You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.