Clinical Director, Clinical Research, Ophthalmology

MSD•Boston, MA

1d•$255,800 - $402,700•Remote

About The Position

The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the ophthalmology therapeutic area. Our company's ophthalmology medicines span all phases of clinical development (pre-clinical to post-licensure). The Clinical Director may manage the entire cycle of clinical development for their assigned studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.

Requirements

M.D or M.D./Ph.D.
Must have experience in industry or faculty in academia
Minimum of 3 years of clinical medicine experience
Minimum of 1 year of industry experience in ophthalmology drug development or biomedical research experience in academia focused on ophthalmology
Demonstrated record of scientific scholarship and achievement
Proven track record in clinical medicine and background in biomedical research
Strong interpersonal skills, as well as the ability to function in a team environment
Strong verbal and written communication and presentation skills
Biomedical Research
Clinical Development
Clinical Documentation
Clinical Investigations
Clinical Medicine
Clinical Reporting
Clinical Research
Clinical Trial Planning
Clinical Trials
Clinical Trial Support
Cross-Functional Teamwork
Drug Development
Early Clinical Development
Ethical Standards
Ophthalmology
Optometry
Regulatory Requirements
Research Methodologies
Scientific Publications

Nice To Haves

Board Certified or Eligible in ophthalmology or related discipline
Prior specific experience in clinical research
Prior publication

Responsibilities

Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy
Medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs
Analyzing and summarizing clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication
Participating in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds
Supporting business development assessments of external opportunities
Actively engage with other functional areas in support of study execution
Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects
Assist the team in ensuring that other colleagues are informed of the progress of studies of our company and competitors' drugs
Provide expert opinion, internally and externally, on relevant scientific questions within their responsibility
Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies
Identifying scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs
Establishing communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of our company's drugs
Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility
Author detailed development documents, presentations, budgets, and position papers for internal and external audiences
Facilitate collaborations with external researchers around the world

Benefits

medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays
vacation
compassionate and sick days

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