Medical Research Specialist

Biogen

. Set strategy for Biogen China study execution and publication .

Posted 9/21/2026full-timeShanghai • ChinaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research and study management, with a strong focus on protocol development, vendor management, and compliance with GCP and SOPs. Proficient in both English and Chinese, facilitating effective communication in diverse, cross-functional teams.

Highest-signal resume keywords

Clinical Research ExperienceProject ManagementProtocol DevelopmentVendor ManagementBilingual Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical StudiesData GenerationStudy Operations ManagementGCP ComplianceSOP DevelopmentFeasibility AssessmentsPublication StrategyData AnalysisQuality Risk ManagementAudit Preparation

Soft Skills

Team CollaborationCustomer OrientationCommunication Skills

Tools & Technologies

MARS Study Tracking System

Industry Keywords

Life SciencesPharmacyClinical ResearchInvestigator-Initiated StudiesPost-Marketing ResearchPhase IV StudiesScientific Publications

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Set strategy for Biogen China study execution and publication
Collaborate with medical managers on data generation for medical-initiated and investigator-initiated studies
Develop and update local affiliate SOPs, protocols, feasibility assessments, and conduct Phase IV, IIT, and other studies
Manage study operations and accountability according to protocols, contracts, GCP, SOPs, and applicable laws
Establish and maintain China study SOPs, handbooks, and clinical operations guidance aligned with global SOPs
Develop protocols for Biogen China-sponsored studies with TA Medical
Serve as primary contact for China data generation communications and collaborate with global and regional functions
Support milestone achievement and manage study issues with cross-functional Biogen teams
Manage study submissions, governance processes, and the MARS study tracking system
Select and manage vendors, ensure study quality, and provide vendor training and materials
Coordinate vendor contracts and payments for post-marketing research activities
Identify study quality risks and implement corrective and preventive action plans
Manage site quality, supervise project CRAs, and monitor deliverables
Lead study audit preparation
Define publication objectives, strategy, and timelines
Coordinate local study data analysis with global medical and publication resources
Manage publication-related processes and projects with global publication teams and local TA
Ensure local vendors complete data analysis accurately and on time
Select publication vendors and ensure compliance with Biogen requirements and standards
Align local publication SOPs with applicable global SOPs

Requirements

What you’ll need

Bachelor’s degree in Life Sciences, Medicine, Pharmacy, or a related scientific discipline preferred
Minimum 2 years of experience in clinical research, clinical studies, and/or scientific publications
Relevant clinical experience required
Proven project management experience with the ability to manage multiple priorities and stakeholders
Excellent written and verbal communication skills in both English and Chinese
Good team player; able to fit into an international, diverse, teamwork culture
Strong customer orientation in science-based work

Benefits

Comp & perks

Learning, growth, and opportunities to expand skills
Inclusive and belonging-focused workplace culture
Opportunities to make significant individual contributions
Stability and resources of a well-established biotechnology company