Sales Manager

Degree: Bachelor’s or above    Location：Hangzhou, Shanghai, Wuhan

Job Responsibilities

1. Identify and analyze customer requirements, hold the market tendency, maintain existing and develop new customer, take care of customer relations, and establish and maintain of new market sales channels.
2. According to customer needs, develop personalized marketing plans, negotiate with customers and achieve cooperation.
3. Attention and internal company the functional departments of the coordination, prompt response and effectively solve the problems and emergencies before and after the launch of project, timely deal with customer complaints, feedback, suggestions, etc., to improve customer satisfaction.
4. Fully excavate potential of itself, gather front-line marketing information, customer opinions, market information, competitor information, etc., raise constructive reference opinions, and spreads business enterprise principle of management, builds up business enterprise popularity and molds business enterprise image.

Job Qualifications

1. Bachelor’s or above in clinical medicine, Pharmacy or other relevant majors.
2. With at least one year working experience and the working experience in CRO is an advantage.
3. Good English reading, writing and speaking skills, and excellent communication skills, both oral and written.
4. Patient and Stringent careful attitude toward work.
 
Please send your CV to HR@deltacro.com. We'll contact you as soon as possible.

Medical Writer

Degree: Master or above    Location：Hangzhou, Shanghai, Wuhan

Job Responsibilities

1. Be responsible for writing Clinical Trial protocol, investigator brochure, informed consent form, CRF, PPT draft design.
2. Be responsible for organize project research, and provide medical support for the company's ongoing clinical research projects, update the Clinical Trial protocol and relevant document version.
3. Participate in the Clinical Trial Protocols seminar, summing-up meeting, and provide relevant academic support.
4. Be Responsible for the interpretation of efficiency and safety in clinical trial.
5. Provide corresponding medical suggestions on the Clinical Trial Protocols and the problems existing in the process.
6. Other responsibilities as assigned.
 

Job Qualifications

1. Master or above in Clinical pharmacy, pharmacology, clinical medicine or other relevant majors.
2. Fluent in written and verbal English,  Proficient in searching and reading English medical and pharmaceutical literature.
3. Familiar with clinical trial design and the related working experience in CRO is an advantage.
4. Familiar with drug registration regulations, GCP and clinical research regulations.
5. Good team work spirit and strong sense of responsibility.
 

Please send your CV to HR@deltacro.com. We'll contact you as soon as possible.

 

Medical Safety Officer

Degree: Master or above    Location：Hangzhou, Shanghai, Wuhan

Job Responsibilities

1. Responsible for medical review of serious adverse events and non-serious adverse events from spontaneous and regulatory authorities report, and support Sponsor review the medical literature of drug safety activities during post-marketing.
2. Medical review of assigned cases to include: review of narrative, coding (e.g. MedDRA) and accurate assessment (seriousness, expectedness, listedness, relatedness) of Adverse Events (serious and non-serious) and of Adverse Drug Reactions (serious and non-serious).
3. Write medical query and similar event analysis and provide casualty assessment for individual case.
4. Weekly Review the list of non-serious events to identify there is any possibility of upgrading to serious cases, and provide medical guidance for triage personnel.
5. Review and use of Clinical Trial Protocols, Product Information, Company Core Data Sheet and any other product related information needed in the course of assigned project.
 

Job Qualifications

1. Medical background, a master degree of clinical medicine in a certain therapeutic area, familiar with the knowledge of the clinical practice in one therapeutic area at least, GCP and the SOP of clinical study.
2. 0-2 years plus clinical research or clinical experience preferred (0-2 years of Pharmacovigilance / Drug Safety experience preferred).
3. Fluent in written and verbal English.
 

 
Please send your CV to HR@deltacro.com. We'll contact you as soon as possible.