东莞招聘

POSITION SUMMARY: 
 The Associate Medical Writing Scientist:

? Learns the medical writing role and pharmaceutical industry and business.
? Learns to work in a team environment and matrix.
? Learns internal standards, regulatory, and publishing guidelines.
? Learns internal systems, tools, and processes.
? Helps to prepare sections of documents and prepares basic documents (therapeutic area-specific) (see examples under "principal responsibilities") under close supervision (is closely trained/coached by a senior-level writer or manager).
? Assists with routine tasks per established procedures (see examples under "principal responsibilities").

PRINCIPAL RESPONSIBILITIES: 

? Helps prepare sections of documents or write basic documents under close supervision such as table of studies, narratives, simple protocol amendments, simple IB updates, IB addenda.
? May assist with document QC, abbreviations, references, literature searches, table creation, and other basic tasks.
? Attention to accuracy, format, and consistency.

DECISION-MAKING AND PROBLEM SOLVING: Describe the types of decisions that are made, reviewed or referred. Describe the types of problems solved or referred. Indicate the degree to which decisions made and problems solved are circumscribed by procedure, policies, standards, or regulations.
Decision making includes: Learns how to interpret, summarize, and present statistical and medical information.

RESPONSIBILITY FOR OTHERS (If applicable): Not Applicable.
ADDITIONAL RESPONSIBILITIES:
1. Learns and adheres to SOPs, templates, best practices, policies, Medical Writing Style Guide.
2. Regularly meets with manager and mentors, and attends departmental meetings.
3. Attends cross-functional meetings with other writers as appropriate (eg, project kick-off and review meetings).
4. Completes all time reporting, training, and metrics database updates as required.
This is not an exhaustive, comprehensive listing of job functions. May perform other duties as assigned.
EMPLOYEES SUPERVISED: CHECK ALL RELEVANT

PRINCIPAL RELATIONSHIPS: Describe the primary working relationships (internal & external) and primary interfaces.
Functional Contacts Inside the Company (as collaborator and peer): manager, peer writers. Getting acquainted with employees from other departments such as Global Clinical Development Operations, Quantitative Sciences, BioResearch Quality & Compliance; External Alliances; TA staff (Clinical).

EDUCATION AND EXPERIENCE REQUIREMENTS: Describe the minimum knowledge, skill and ability requirements for the position. Include any degrees or certifications which are required and/or desirable.
A university/college degree is required. An advanced degree (eg, Masters, PhD, MD) is preferred. No relevant pharmaceutical experience is required.

QUALITIES AND CHARACTERISTICS:
? Solid oral and written communication skills.
? Attention to detail.
? Ability to function in a team environment.
? Organizes time well with short-term responsibilities.
? Demonstrates learning agility.

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