Clinical Planning Analyst

3 days ago

Petaling Jaya, Malaysia IQVIA Full time

Reporting into Director of Clinical Planning & Analytics, you will manage and co-ordinate activities for assigned opportunities and projects, in performing data mining and analysis, formulating recommendations and presenting to internal and potentially external stakeholders.

**Key Responsibilities**:

- Accountable to ensure IQVIA planning services are providing a competitive edge in winning new business. Take independent responsibility for IQVIA commitments of future studies by delivering accurate and robust country, site or enrollment strategies in support of opportunities including but not limited to requests for proposals, early engagements, re-bids and potentially awarded studies.
- Support the development of materials related to feasibility or site lists or enrollment strategies for customer bid defense meetings or internal customers such as Therapeutic Strategy Leads, Medical Leads or business development
- Collaborate with key stakeholders and IQVIA project teams to resolve issues
- Prepare for planning meetings by conducting research into therapeutic areas using databases, scientific literature, the internet and expert medical knowledge
- Lead planning meetings with internal stakeholders including Medical Directors, Therapeutic Strategy Leads, Business Developers, Sales Staff and Program Directors. Present results of data gathering and analysis activities.
- Undertake therapeutic training, as necessary, and keep abreast of developments in clinical research
- Train and support new team members.
- Proficient with planning tools, demonstrate an in depth understanding of system features and functions to know what features are best used to accomplish an accurate country, site or enrollment strategy.

**Key Requirements**:

- Bachelor's Degree in Healthcare or Biological Science
- 3 years related experience in clinical research. Equivalent combination of education, training and experience.
- Clinical/project management experience is preferred.
- General knowledge and understanding of company clinical systems, procedures and corporate standards.
- Good knowledge of medical terminology, GCP, FDA regulations, and Drug Development process.
- In-depth understanding of clinical research.
- Excellent communication, organizational and interpersonal skills.
- Fluid report writing in English
- Strong computer literacy, including well-developed computer skills in applicable software.
- Ability to work independently and effectively prioritize tasks.

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