- Company Name
- Veristat
- Job Title
- Senior Project manager
- Job Description
-
**Job Title:** Senior Project Manager
**Role Summary:**
Leads planning, preparation, and execution of multiple complex, high‑profile clinical research projects. Acts as primary liaison among internal functional teams (clinical monitoring, data management, biostatistics, pharmacovigilance, medical writing, business development, compliance, leadership) and external sponsors and vendors. Ensures projects meet regulatory, timeline, and quality objectives.
**Expectations:**
- Deliver projects on schedule, within budget, and compliant with ICH GCP and other regulations.
- Build and motivate cross‑functional project teams; mentor junior staff.
- Communicate clearly with clients, vendors, and internal stakeholders.
- Navigate a fast‑paced environment with resilience and decisive action.
**Key Responsibilities:**
- Develop and maintain comprehensive project plans, timelines, and budgets.
- Coordinate day‑to‑day activities across clinical monitoring, data management, SAS programming, biostatistics, pharmacovigilance, and medical writing.
- Manage stakeholder relationships, including sponsors, external vendors, and internal leadership.
- Monitor regulatory compliance and ensure adherence to ICH GCP and related guidelines.
- Produce and present status reports, risk assessments, and mitigation strategies.
- Lead project meetings, drive decision‑making, and resolve escalated issues.
- Mentor team members and delegate tasks effectively.
**Required Skills:**
- Proven clinical trial project management (3+ years) in CRO or pharmaceutical setting.
- Strong knowledge of ICH GCP, regulatory requirements, and medical terminology.
- Excellent written and verbal communication in English.
- Superior organizational, interpersonal, and leadership abilities.
- Ability to manage multiple projects simultaneously and prioritize tasks.
- Proficient in risk management, budgeting, and resource allocation.
**Required Education & Certifications:**
- Bachelor’s degree in life sciences, health sciences, or a related discipline (or equivalent experience).
- Minimum 6–8 years overall clinical research experience, with at least 3 years in project management.
- Relevant certifications (e.g., PMP, PRINCE2) are advantageous but not mandatory.