Urgent Search: Clinical Data Manager
2 weeks ago
Position:
Clinical Data Manager
Requirement:
Immediate Joiner
Location:
Hyderabad only
Experience: 5 to 10 Years only
Key Roles & Responsibilities:
- Provide leadership and vision to the team.
- Manage and deliver largescale, highcomplexity studies across a range of sponsors and therapeutic areas.
- Manage sponsors at both the study and program levels.
- Ensure milestones meet timelines and quality deliverables.
- Provide project management expertise, working with customer data managers, key decisionmakers, and internal team members to manage continuous process improvements and provide technical expertise.
- Conduct performance reviews, establish annual expectations for the team, and provide coaching and development as needed.
- Strategically monitor workload volume and ensure task assignments are balanced across the team to meet key deadlines and sponsor expectations.
- Ensure team members meet established quality and performance standards and recommend additional performance standards.
- Achieve growth, hit revenue targets, and foster organizational development.
- Establish, cultivate, and maintain strong, longterm relationships with clients and their sponsors; identify, develop, and implement process improvement and outreach plans, presentations, and strategies designed to grow partnerships between clients and IQA.
- Identify skill and competency gaps at the individual level and work to craft development plans that will close these gaps.
- Actively engage with industry events to gather intelligence, enhance public perception, and market penetration of IQA services and products; provide training on industry intelligence back to internal teams.
- Develop, implement, and measure marketing plans for IQA products and services, targeting priority segments and geographies.
- Identify and create marketing content requirements with stakeholders across the organization.
- Maintain high visibility within customer organizations. Monitor customer satisfaction by communicating regularly with the customer.
- Provide innovative ideas and strategies to compete with global CROs by developing solutions and products.
- Identify use cases to leverage technologies like R, Python, & Julia in clinical trials.
- Identify opportunities for AI & ML in clinical trials.
- Increase IQA visibility by attending conferences, presenting, and publishing papers in national/international scientific journals, and writing technical/functional blogs.
- Interact with industry SMEs and universities to establish a global forum for clinical research technologies.
Qualifications:
- Bachelor's or master's degree in Life Sciences, Biostatistics, Computer Science, or related field.
- Proven experience in clinical data management in a pharmaceutical or CRO environment.
- Strong knowledge of data management practices and regulatory guidelines (e.g., GCP, ICH).
- Proficiency in data management software and tools (e.g., EDC systems, SAS).
- Excellent organizational, communication, and problemsolving skills.
- Ability to work collaboratively with multiple teams and manage multiple projects simultaneously.
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