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Clinical Director, Clinical Research - Lymphoma
MSDClinical Director at a global healthcare leader responsible for planning clinical research for new and marketed Oncology medicines. Managing clinical trials and leading cross-functional collaboration.
Posted 6/17/2026full-timeRahway • Massachusetts, New Jersey • 🇺🇸 United StatesLead💰 $255,800 - $402,700 per yearWebsite
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
clinical researchstudy designclinical development planIND applicationsclinical trialsdata analysisregulatory reportingscientific writingbudget managementclinical monitoring
Soft Skills
interpersonal skillsteam collaborationleadershipcommunicationstrategic planningproblem-solvingsupervisionpresentation skillsscientific knowledgeproject management
Certifications & Qualifications
M.D.M.D./Ph.D.
Industry Keywords
OncologyAdult Lymphomabiomedical researchclinical medicinedrug developmentclinical trials managementscientific scholarshiptranslational researchresearch project teamsclinical findings analysis
About the role
Key responsibilities & impact- Planning and directing clinical research activities involving new or marketed Oncology medicines
- Manage the entire cycle of clinical development, including study design, initiation, monitoring, analysis, regulatory reporting, and publication
- Evaluating pre-clinical and translational work for generating clinical development plan and IND applications
- Developing clinical development strategies
- Planning clinical trials based on strategies
- Monitoring and managing ongoing or new clinical trials
- Analyzing and summarizing clinical findings from studies
- Participation in internal and joint internal/external research project teams
- Supervise Clinical Scientists in study execution
- Work with a cross-functional group of experts to manage clinical development
- Assist the Senior/Executive Director in ensuring corporate personnel are informed of study progress
- Maintain strong scientific fund of knowledge
- Author development documents, presentations, and budgets
- Facilitate collaborations with external researchers
Requirements
What you’ll need- M.D or M.D./Ph.D.
- Minimum of 3 years of clinical medicine experience
- Minimum of 1 year of industry experience in drug development or biomedical research or experience in academia
- Expertise in Adult Lymphoma
- Demonstrated record of scientific scholarship and achievement
- A proven track record in clinical medicine and background in biomedical research is essential
- Strong interpersonal skills, as well as the ability to function in a team environment are essential.
Benefits
Comp & perks- Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family)
- Retirement benefits, including 401(k)
- Paid holidays
- Vacation
- Compassionate and sick days.