Clinical Data Manager and Project Manager

CDM PM

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Data Manager Project Manager – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

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.

What You’ll Do:

• 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. Additionally, 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.

Education and Experience Requirements:

• • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• • 8+ Years of experience in Clinical Data Management
• Should have experience in Veeva EDC
• Should have worked in End to End - Study Strat up, Conduct and Close Out Activities
• Should have experience in Resource Capacity Management, Project Finance/Billing, Training, Audit related activities
• Should have experience sponsor/Client Management

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.

Knowledge, Skills and Abilities:

• • 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.

Why Join Us?

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.

Apply today to help us deliver tomorrow’s breakthroughs.

Experience Level

Senior Level