# Senior Clinical Data Manager – FSP / oncology experience

**Company**: Fortrea
**Location**: Maidenhead
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/Senior-Clinical-Data-Manager---sponsor-dedicated---oncology_263545?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_ac2be21c-43b

## Description

We are seeking a Senior Clinical Data Manager to join our team. As a Senior Clinical Data Manager, you will be responsible for the full cycle of Clinical Data Management queries, from leading studies and being the main point of contact with clients, to hands-on tasks such as creating eCRFs, cleaning data, and performing set-up to close-out duties.

You will work in a highly collaborative environment with other Clinical Data Managers, Data Coordinators, Statistical Programmers, and others.

**Responsibilities**

- Provides CDM leadership for one or more assigned projects or indications dependent on size and scale of the project.

- Lead studies including a combination of healthy volunteer and patient populations, multi-site, complex protocol design, strong client management required or reduced timelines.

- Demonstrates leadership and operational expertise in the strategic planning and delivery of CDM deliverables at program and/or project level.

- Management and oversight of vendor contracts, resourcing and budget management and oversight of vendor performance for assigned programs, and projects.

- Communicates and negotiates effectively with all other Program level team members.

- Provide oversight and expertise of external service providers or in-house teams to deliver quality data with compliance to study model procedures and standards.

- Responsible for proactive risk management and issue resolution/escalation connected to Clinical Data Management improvement or technology.

- Develops an understanding of CDASH and SDTM or other recognized industry standards and impact to programming team to ensure consistency of program level standards.

**What you can expect from us**

- Office based or home based anywhere in the listed countries.

- Exposure to high profile global studies.

- Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.

- A genuine work-life balance.

- Flexibility in working hours.

- A thorough onboarding with support from your personal mentor.

**Your profile**

- University/college degree (life science, pharmacy or related subject preferred).

- 8 years of combined early or late-stage DM experience with minimum 2 years of direct sponsor management and at least 2 years technical mentoring experience.

- Extensive experience in clinical data management and experience leading studies in a CRO/Pharma setting.

- Understanding of RECIST criteria.

- Excellent oral and written communication and presentation skills.

- In-depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.

- Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical/biotechnological companies.

## Skills

### Required
- Clinical Data Management
- CDM leadership
- study management
- client management
- data analysis
- CDASH
- SDTM

### Nice to have
- oncology experience
- RECIST criteria
- clinical trial process
- biometrics
- quality management

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/Senior-Clinical-Data-Manager---sponsor-dedicated---oncology_263545?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)