Clinical Development Trial Lead (CDTL)
mindlanceIndianapolis (IN)
Clinical Development Trial Lead (CDTL)
Posted 24 days ago
mindlanceIndianapolis (IN)
SENIORITY
Manager
About the role
Job-ID28604159Reference26-16786 Openings & Locations 4-5 total openings 3 positions based in Indianapolis, IN 2 positions based in Stamford, CT Preference for candidates who can work onsite at either location Strong remote candidates may be considered, particularly those with significant Big Pharma experience Position Overview Client is seeking experienced Clinical Development Trial Leads (CDTLs) to support global oncology clinical trials across both early and late-stage development programs. The majority of openings are focused on Early Phase Oncology, with 1-2 positions supporting Late Phase studies. The CDTL will function as an independent study leader responsible for end-to-end clinical trial management and operational execution of global oncology studies involving solid tumor indications. This role requires strong leadership, cross-functional collaboration, vendor oversight, and project management capabilities. Therapeutic Area Oncology Solid Tumor Indications Study Phase Majority Early Phase (Phase I Oncology) Limited Late Phase opportunities Geographic Scope Global clinical trials conducted across: North America Europe APAC Travel Requirements Less than 10% travel Occasional travel to Ireland may be required Key Responsibilities Lead end-to-end clinical trial management activities from study start-up through closeout. Independently manage complex global oncology studies. Partner closely with Program Leads and cross-functional teams to ensure successful study execution. Oversee and drive CRO performance, ensuring accountability for study deliverables, timelines, and quality. Manage external vendors and strategic partners involved in study execution. Lead and participate in Study Management Team meetings. Collaborate with Data Management, Clinical Operations, Regulatory Affairs, Medical, Safety, and other functional teams. Monitor study progress, identify operational risks, and drive mitigation strategies. Support both development and post-marketing clinical trial activities where applicable. Ensure studies are conducted in compliance with GCP, regulatory requirements, and company standards.
Required Qualifications:
Minimum 5 years of direct Oncology clinical trial experience. Strong experience in end-to-end Study Management. Experience leading global clinical trials across multiple regions. Proven ability to work independently with minimal supervision. Experience managing CROs, vendors, and external partners. Strong cross-functional leadership and stakeholder management skills. Solid project management experience. Experience supporting study start-up, study conduct, data management activities, and study closeout. Preferred
Qualifications:
10 years of Oncology clinical development experience. Significant experience in Early Phase Oncology (Phase I studies). Experience with Solid Tumor programs. Background within both Big Pharma and CRO environments. Experience operating at the Senior Manager or Associate Director level. Ability to manage highly complex global studies and influence stakeholders across functions. Team Environment Approximately 30 professionals within the Early Phase Oncology group. Highly collaborative yet independent working environment. Candidate will serve as a key operational leader with significant ownership and accountability. Frequent interaction with Program Leads, CRO Project Managers, and cross-functional stakeholders.
Interview Process:
Round 1 Panel Interview (90-120 minutes) Both of the Early Phase managers and Late Phase Managers Additional member(s) of the management team Final Round Leadership Interview (90-120 minutes) VP AVP Candidates who successfully clear the panel interview will advance to the leadership discussion.
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