Associate Clinical Data Manager

Fortrea is expanding its Clinical Data Management team and we're looking for an Associate Clinical Data Manager to join our FSP model. This is a unique opportunity to be part of a growing footprint in the region and contribute to global clinical trials from the start-up phase. Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study start-up to database lock) according to client quality expectations, within project timelines and budgets. Work directly with Sponsors to understand their direct requirements and lead implementation of those requirements. Regularly review client specific process to ensure they remain optimal for Sponsor and Fortrea. Summary of Responsibilities: Lead studies including (but not limited to) a combination of healthy volunteer and patient populations, multi-site, client management required or reduced timelines. Ability to organize and effectively prioritize workload and deliverables. Be accountable for all DM deliverables as assigned per the established timeline; providing instruction to their DM study team(s) and review of their study team’s output to ensure the highest quality, while adjusting resource allocations accordingly. Ensure that all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCPs. Work with the Project Manager(s) to build timelines to meet contracted milestones by communicating with leads in different disciplines and the full project team as necessary, including at study initiation meetings. Provide DM project team leadership and accountability; leads data focused internal project team meetings; meets frequently with the study leads of EDC Design, SAS Programming, Statistics, and PK to ensure that all deliverables are planned and coordinated intradepartmental; proactively identifies potential risks/mitigations, effectively communicates data-driven discussions in order to achieve database lock dates; keeps the Project Manager apprised of project progress. Maintain awareness of other Biometrics functional group deliverables to be able to support risk and mitigation strategies, including impact on DM resources or deliverables and consult with Project Manager (or designee) and/or functional group management as necessary. Keep Project Manager (or designee), Biometrics management team and/or sponsor services informed of pertinent project or sponsor related information (i.e., budget status, work scope changes, timeline impacts). Performs other related duties as assigned by Line Management. Develop and maintain client relationships and review client satisfaction surveys. Track scope changes and work with the Project Manager to ensure that Sponsor approval is received, and the scope change processed. Provides leadership, mentorship, and coaching in DM related clinical trial processes to the internal study team. Provide support to DM managers on the performance evaluation of other team members, provide constructive feedback to aid in career development, interpersonal skills and achievement of competency standards. Accountable for learning new DM technologies and applied processes, keeping up to date with industry wide technology and feasibility for process improvement at Fortrea. Maintain accurate records of all work undertaken. Perform reconciliation of the clinical database against safety data, laboratory data or any other third-party data as appropriate. Utilize local laboratory systems and batch data load facilities where appropriate. Represent DM and where necessary overall Biometrics in new business opportunities. Attend and action client or internal audits as appropriate and resolve all issues within an appropriate timeframe. Address client comments with the study team. Actively promote Biometrics services to sponsors whenever possible. All other duties as needed or assigned. Minimum Qualifications: University degree in Life Sciences, Health Sciences, Information Technology, or a related field. Equivalent experience in clinical research or data management may be considered in lieu of a formal degree. Fluent in English, both written and verbal. Knowledge of science or a scientific background. Experience (Minimum Required): 2–4 years of experience in clinical data management or related roles. Understanding of GCP, ICH guidelines, and clinical trial processes. Knowledge of Data Management, Clinical Operations, Biometrics, and system applications to support operations. Familiarity with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle InForm, Veeva Vault) Experience working in cross-functional teams and supporting global stakeholders. Strong organizational and time management skills with the ability to meet project productivity metrics and timelines. Effective communication and interpersonal skills, with a collaborative and team-oriented mindset. Demonstrated attention to detail and strong documentation skills. Ability to handle customer concerns and support scope of work and budget discussions. Knowledge of medical terminology. Comfortable working in a fast-paced, metric-driven environment. Ability to work effectively in a remote, multicultural, and cross-time-zone environment.

Preferred Qualifications

Include:

• Prior experience in FSP or CRO environments is a plus.
• 3+ years of Electronic Data Capture (EDC) experience.

Work Environment:

• Office and home-based work environment.
• May require occasional evening or weekend work to meet global timelines.
• Flexible shifts may be required to support international teams.

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