Content Analyst(Lifescience function)

Patsnap; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A global pharmaceutical consultancy in Singapore is looking for Content Analysts to join their content team. You will be responsible for collecting and organizing pharmaceutical data, standardizing intelligence systems, and collaborating with IT. The ideal candidate has a Master’s degree in Biology or Pharmaceutical Sciences with some relevant experience. This full-time role offers an entry-level position with opportunities to provide insights on industry hotspots.

Qualifications

• 0-3 years of relevant experience in a pharmaceutical company.
• Ability to communicate clearly and concisely in both written and spoken English.
• Proficiency in using pharmaceutical databases preferred.

Responsibilities

• Collect and organize global pharmaceutical data from regulatory websites.
• Standardize pharmaceutical data intelligence systems and maintain drug data.
• Collaborate with the IT team for data handling rules and produce requirement documents.
• Provide insights on pharmaceutical R&D hotspots or industry pain points.

Skills

Analytical skills

Communication skills

Problem identification and solving

Education

Master’s degree in Biology, Pharmaceutical Sciences or related field

Job description

Job Summary

We are looking for Content Analysts to join our content team in Singapore. This is an amazing opportunity to be a member of a talented global team. We have great knowledge in pharmaceutical research and would love to speak with you if you have skills in biology, medicinal chemistry.

About You

• Educational Qualification: Master’s degree (M.Sc.) in Biology, Pharmaceutical Sciences, or a related field required; an advanced degree is preferred.
• Relevant experience of (0-3 years) in a pharmaceutical company, ideally in the life science related software or information services industry, problem identification and solving skills, good analytical skills.
• Outstanding communication skills (written and oral) with ability to communicate clearly, concisely, and objectively in both written and spoken English.

It would be great if you also had

• In-depth knowledge of drug R&D, regulatory and policies; experience in pharmaceutical information research and project initiation is preferred.
• Proficiency in using pharmaceutical databases, with the ability to query global regulatory website databases and professional websites.

What will you be doing in this role?

• Responsible for collecting and organizing global pharmaceutical data, tracking information from regulatory websites of major jurisdictions (China, U.S., EU, Japan, etc.), global pharmaceutical news, conferences, etc., to obtain information on drug clinical progress, registration, approvals. Ensuring data is updated accurately and promptly.
• Participate in standardizing the pharmaceutical data intelligence system, familiarizing with annotation systems for targets, indications, etc., and maintaining drug data based on reliable pharmaceutical intelligence.
• Collaborate with the IT team to develop rules for data crawling, cleaning, and annotation, and produce requirement documents.
• Utilize individual expertise to provide insights on pharmaceutical R&D hotspots or industry pain points.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Management and Manufacturing

Industries

• Software Development

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