Position overview
United Research Group is seeking a Clinical Development Manager to support clinical development planning, study strategy, and cross-functional execution of clinical research programs.
The position will collaborate with investigators, sponsors, CROs, and internal stakeholders to support clinical development objectives, operational feasibility, and high-quality study delivery.
Responsibilities
- Support clinical development plans and study execution strategies.
- Collaborate on protocol feasibility, study design considerations, and operational planning.
- Coordinate with clinical operations, medical oversight, regulatory, and data management teams.
- Monitor development milestones, timelines, and study progress.
- Identify clinical development risks and recommend mitigation strategies.
- Support investigator and research-site feasibility assessments.
- Participate in study planning and cross-functional review meetings.
- Contribute to clinical study reports and development documentation as assigned.
- Support sponsor and CRO communications.
- Maintain alignment with applicable GCP and regulatory requirements.
The qualifications below are proposed recruitment criteria pending final URG approval.
Proposed qualifications
- Bachelor's degree in life sciences or a related discipline preferred; advanced degree desirable.
- Approximately 5 or more years of relevant clinical development, clinical operations, or clinical project management experience preferred.
- Experience supporting clinical trials across one or more therapeutic areas.
- Knowledge of clinical development processes, ICH-GCP, and applicable regulatory requirements.
- Strong project coordination, analytical, and communication skills.
- Experience collaborating with cross-functional and geographically distributed teams.
- Ability to work independently in a remote environment.