Associate Director of Clinical Data Management
London, England
Overview
Your work will change lives. Including your own.
The Impact You’ll Make
Recursion is seeking an Associate Director, Clinical Data Management who can lead and oversee end to end Clinical Data Management activities on assigned studies and programs. You’ll manage all 3rd party data sources and serve as SME for Data Management. You’ll lead and deliver initiatives for CDM within the Biometrics group and collaborate with cross functional groups within the Clinical Development organization and larger Data Science teams at Recursion. You will be responsible for all the CDM study activities and deliverables, document reviews, oversight of CROs, timelines and project risk management. You can expect to work on multiple projects in a fast-paced environment.
In this role, you will:
* Lead End to End Data Management activities with hands on ability to manage outsourced studies and lead DM and external vendor oversight activities and deliverables. Proficiency in project management leading 3-4 outsourced programs, simultaneously.
* Represent Data Management function in Clinical Study Meetings, ensuring proactive alignment of expectations between the CRO and Recursion regarding all data-related deliverables.
* Work with CRO and Recursion functional groups to complete EDC setup, database migrations / UAT and other systems such as IRT, ePRO etc. Manage multiple vendor sFTPs for data retrieval and delivery to stat programming, routinely.
* Establish Vendor Oversight Plans for all studies and responsible for Vendor Data Quality Reviews and Oversight. Harmonize processes where relevant with other Recursion clinical programs.
* Serve as a SME for various operational activities and DM processes like EDC, External data standardization, Collection, and Processing. Lead efforts with Biometrics and Clin Dev for creation and standardization of CRFs and Data Review Plans. Routinely provide study metrics, planning of deliverables, and propose solutions for data handling/related issues.
* Lead/Oversee the creation and maintenance of Data Management documents including, but not limited to, CDMP, CCGs, Data Review Plans, edit checks, Listing review checks, Data Integrations specs, Data Transfer Specs, External Data Reconciliation plans, SAE Reconciliation Guidelines, Coding Guidelines, Database Lock, Checklists and Plans.
* Coordinate with vendors to guarantee data collection is compatible with clinical databases and meets SDTM requirements.
* Strategic and critical thinker who can independently lead initiatives and collaborate cross functionally.
* Accountable for coordination with other functional groups for submission related activities.
* Manage strategic input into the design of data flow across EDC and non-EDC data sources across vendor networks.
* Ensure filing, archival and inspection readiness of all Data Management Trial Master File (TMF) activities.
* Review and manage external Data Management Budgets, ensure accuracy, and understand trends to support Budget planning and forecasting.
* Support the development of Clinical Data Management Standard Operating Procedures and Work Instructions.
* Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and CDM guidance documents.
The Team You’ll Join
Reporting to Senior Director, Clinical Data Management and working closely with Biometrics, Clinical Operations and Clinical Development Organization, you will be an essential member of the Recursion Development Team. The Development Team is an empowered, execution-minded group of drug development professionals responsible for translating Recursion’s innovative science to patients through clinical development activities.
The Experience You’ll Need
* Bachelor’s degree in science, math or computer science
* 12+ years’ experience in the biopharmaceutical industry. Experience, technical proficiency and People management skills will determine the level.
* Experience managing external data and 3rd party vendors is a must.
* Strong knowledge of regulations and guidelines that apply to the conduct of clinical trials.
* Excellent written and verbal communication skills and ability to work collaboratively as a part of a team.
Working Location & Compensation
This position can be based at any of our offices in London or Oxford. We are a hybrid environment and ask that employees spend 50% of their time in the office. Relocation support can be provided. The estimated current annual base range for this role is:
* £84,000- £98,900 GBP for candidates based in the United Kingdom
You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package.
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The Values We Hope You Share
* We act boldly with integrity. We are unconstrained in our thinking, take calculated risks, and push boundaries, but never at the expense of ethics, science, or trust.
* We care deeply and engage directly. Caring means responsibility and respect - showing up, speaking honestly, and taking action.
* We learn actively and adapt rapidly. Progress comes from doing. We experiment, test, and refine, embracing iteration over perfection.
* We move with urgency because patients are waiting. Speed is about moving the needle every day.
* We take ownership and accountability. Leaders take decisive action; teams own outcomes together.
* We are One Recursion. True cross-functional collaboration is about trust, clarity, humility, and impact.
Our values underpin the employee experience at Recursion. They guide how we communicate, support one another, spend our time, decisions, and celebrate.
Equal Opportunity Employment Information (Recursion)
Recursion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable law. Accommodations are available on request for candidates taking part in the selection process.
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