# Medical Advisor

**Company**: IQVIA
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Shanghai-China/Sr-Medical-Advisor--Medical-Mgr-Sr-Medical-Mgr_R1553556-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_8380c20a-726

## Description

We are seeking a Medical Advisor to join our team.

Responsibilities:

- Prepare and organize discussion activities for various clinical research programs, and closely communicate with principal investigators or experts in the treatment field regarding research programs.

- Responsible for medical writing related to clinical research projects, such as writing clinical research plans and clinical research summary reports, according to company SOPs and client requirements.

- Conduct medical review of projects, including reviewing research plans, informed consent forms, investigator's manuals, case report forms, statistical analysis plans, clinical research summary reports, and medical coding of adverse events.

- Develop medical monitoring plans according to company SOPs and project requirements, ensuring project quality and safety, including but not limited to SAE and protocol deviation monitoring.

- Provide project support to clinical operation teams, including participating in site feasibility assessments, selecting principal investigators, and conducting initial medical discussions with them.

- Provide medical training and support to project teams or investigators, including preparing medical training materials, providing relevant treatment field medical knowledge, and program training.

- Attend investigator meetings to present medical-related content (if needed).

- Participate in project kick-off meetings, research team meetings, and client meetings as needed.

- Provide medical support for new project proposals to the BD team, meeting with clients if necessary to discuss medical issues related to the program.

- Establish good communication relationships with medical experts in key areas, regularly visiting academic experts, updating medical progress information, and maintaining good cooperative relationships with them.

- Write SOPs related to the department as required.

- Establish good cooperative relationships with other departments in the company.

- May require irregular business trips as needed.

- Efficiently complete tasks assigned by direct managers.

Requirements:

- Rich clinical trial knowledge background.

- Understanding of clinical trial-related regulatory requirements, such as China's GCP, ICH-GCP, etc.

- Proficient in using Microsoft Word, PowerPoint, and Excel software.

- Good oral and written communication skills (including proficient English).

- Good presentation skills and training skills.

- Strong collective awareness and good teamwork spirit;

- Ability to establish and maintain effective working relationships with colleagues, managers, and clients.

Education and Experience:

- Bachelor's degree or higher in clinical medicine, or master's degree or higher in pharmaceutical-related majors.

- Bachelor's degree requires 3 years or more of medical advisory or hospital clinical or clinical research experience;

- Master's degree requires 2 years or more of medical advisory or hospital clinical or clinical research experience;

- Doctoral degree requires 1 year or more of medical advisory or hospital clinical or clinical research experience;

- Equivalent education, training, and experience are preferred.

## Skills

### Required
- clinical trial knowledge
- Microsoft Word
- PowerPoint
- Excel
- English

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Shanghai-China/Sr-Medical-Advisor--Medical-Mgr-Sr-Medical-Mgr_R1553556-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)