RESUME AND JOB
MSD
Categories: Pharmaceutical, Research, Biotechnology, Drug Discovery
Job Description
Duties and Responsibilities
Target and program evaluation: Conduct literature and data reviews to identify and prioritize disease-relevant targets and mechanisms of action. Assess scientific rationale, competitive landscape, and translational feasibility for potential internal and collaborative programs. Experimental design and hypothesis testing: Design and refine in vitro and in vivo study plans to evaluate targets, pathways, biomarkers, and candidate agents. Define success criteria, controls, endpoints, and statistical considerations appropriate to each study. External study execution and data tracking: Partner with CROs to execute assays and models; provide protocols, monitor progress, ensure data quality, and manage timelines and budgets. Initiate and manage third-party validation of key findings to de-risk collaborations. Data interpretation and decision support: Analyze and integrate datasets across experiments; summarize findings, visualize results, and develop evidence-based recommendations. Prepare concise reports and presentations for internal reviews and governance milestones.
D.
Key Requirements
Ph.D. in biology, molecular/cellular biology, pharmacology, immunology, oncology, neuroscience, or a related field. Demonstrated research experience in disease biology, target identification/validation, or experimental therapeutics (industry experience optional but welcome). Proficiency in experimental design, assay development, and data interpretation in disease-relevant in vitro and/or in vivo models; familiarity with translational models preferred. Experience with experimental drug evaluation, combination strategy exploration, and CRO collaboration/management is a plus.
Other Requirements
Excellent written and verbal communication skills in Chinese and English. Fast learner with the ability to adapt to diverse project needs and operate in a dynamic, collaborative environment.
Required Skills:
Accountability, Accountability, Analytical Thinking, Assay, Assay Development, Automated Liquid Handling Systems, Bioanalytical Method Development, Bioanalytical Techniques, Biopharmaceuticals, Cell-Based Assays, Clinical Judgment, Data Analysis, Experimentation, Flow Cytometry, Immunoassays, Immunochemistry, Immunohistochemistry (IHC), Immunology, Microbiology, Neuroanatomy, Oncology, Pharmacokinetics, Physiology, Project Reviews, Research Proposal Development {+ 4 more}Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
Not ApplicableShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
noJob Posting End Date:
06/30/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
94,500 - 143,000 USD / yearly
Source: AI Estimation
* This is an estimated range based on market data and may vary based on experience and qualifications.
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MSD
Categories: Pharmaceutical, Research, Biotechnology, Drug Discovery
Job Description
Duties and Responsibilities
Target and program evaluation: Conduct literature and data reviews to identify and prioritize disease-relevant targets and mechanisms of action. Assess scientific rationale, competitive landscape, and translational feasibility for potential internal and collaborative programs. Experimental design and hypothesis testing: Design and refine in vitro and in vivo study plans to evaluate targets, pathways, biomarkers, and candidate agents. Define success criteria, controls, endpoints, and statistical considerations appropriate to each study. External study execution and data tracking: Partner with CROs to execute assays and models; provide protocols, monitor progress, ensure data quality, and manage timelines and budgets. Initiate and manage third-party validation of key findings to de-risk collaborations. Data interpretation and decision support: Analyze and integrate datasets across experiments; summarize findings, visualize results, and develop evidence-based recommendations. Prepare concise reports and presentations for internal reviews and governance milestones.
D.
Key Requirements
Ph.D. in biology, molecular/cellular biology, pharmacology, immunology, oncology, neuroscience, or a related field. Demonstrated research experience in disease biology, target identification/validation, or experimental therapeutics (industry experience optional but welcome). Proficiency in experimental design, assay development, and data interpretation in disease-relevant in vitro and/or in vivo models; familiarity with translational models preferred. Experience with experimental drug evaluation, combination strategy exploration, and CRO collaboration/management is a plus.
Other Requirements
Excellent written and verbal communication skills in Chinese and English. Fast learner with the ability to adapt to diverse project needs and operate in a dynamic, collaborative environment.
Required Skills:
Accountability, Accountability, Analytical Thinking, Assay, Assay Development, Automated Liquid Handling Systems, Bioanalytical Method Development, Bioanalytical Techniques, Biopharmaceuticals, Cell-Based Assays, Clinical Judgment, Data Analysis, Experimentation, Flow Cytometry, Immunoassays, Immunochemistry, Immunohistochemistry (IHC), Immunology, Microbiology, Neuroanatomy, Oncology, Pharmacokinetics, Physiology, Project Reviews, Research Proposal Development {+ 4 more}Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
Not ApplicableShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
noJob Posting End Date:
06/30/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
94,500 - 143,000 USD / yearly
Source: AI Estimation
* This is an estimated range based on market data and may vary based on experience and qualifications.
Get personalized recommendations to optimize your resume specifically for Asso. Manager, MCICC. Takes only 15 seconds!
Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.
Answer 10 quick questions to check your fit for Asso. Manager, MCICC @ MSD.

No related jobs found at the moment.

© 2026 Pointers. All rights reserved.