- Analysts and Implementation Specialists. Physicians are selecting and implementing electronic health/medical record (EHR or EMR) and they need assistance in knowing which EHR to select, how to implement the system, how to modify their current workflow structure, how to train their staff, etc. Look for titles such as Clinical Systems Analyst, Lead Analyst, Informaticist, Implementation Specialist, Health IT Specialist, Pharmacy Analyst, Medical Analyst, Systems Analyst, etc. Many of these jobs are highly technical positions that require you to have a background in engineering, programming, etc.
- Directors and Managers. There will always be a need for managers to oversee projects. So, you may see job titles such as Project Manager, Team Lead, Health IT Director, EHR or EMR Manager, EHR or EMR Director, Director of Health Information Management, Medical Director of Informatics, CMIO, etc.
- Trainers and Application Coordinators. These positions may still be of interest, even though they aren't the most appropriate settings for physicians.
- Consultants. Physicians make great consultants, especially for start-up companies that are entering the health IT space. Do you have what it takes to be an EMR or EHR Consultant? Medical Informatics Consultant. Clinical Informatics Consultant.
Showing posts with label clinical director. Show all posts
Showing posts with label clinical director. Show all posts
Monday, January 4, 2010
Health Information Technology (Health IT) jobs for physicians
Tuesday, May 6, 2008
Director, Clinical Due Diligence - posted 5/6/2008
An executive search firm is looking to hire a a Director/Senior Director-Clinical Due Diligence position within a well known, expanding pharmaceutical company in Mid/Central NJ (full company relocation program). It is an exciting new opportunity that will provide a broad scope of responsibility and visibility within the organization.
Director, Clinical Due Diligence
SUMMARY:
Reports to the Chief Medical Officer, the Director of Clinical Due Diligence is charged with onsite and offsite review of clinical opportunities in collaboration with business development. Individual is intended to work with business teams in evaluating potential business deals from medical and clinical research perspective. Will be required to meet and counsel executive leadership.
RESPONSIBILITIES:
Provides business development leadership team medical and clinical due diligence of candidate early development to post-marketed products
Travel with team for due diligence of business licensing candidates
Working knowledge of pharmacovigilance and risk management activities
Participate in product development meetings
Prepare/deliver presentations on medical perspective
Evaluate in-license pharmaceutical candidates
Assess qualitative and quantitative composition of in-vitro and in-vivo product performance
Attend professional conferences and meetings
REQUIREMENTS:
Understand clinical development of pharmaceutical drug products, modeling and population PK analyses
Excellent interpersonal skills, self-motivation, and positive attitude
Analytical skills as well as excellence in oral and written communications
Ability to review business development projects
Have experience in medical affairs and clinical research
Ability to handle multiple issues on multiple projects simultaneously.
Ability to maintain a high degree of independence with respect to decision making and problem solving
Liaise with other departments/ divisions to ensure successful outcome in due diligence of projects
Strong negotiating skills
Must have ability to analyze and evaluate processes and procedures
Previous experience in business development
Clinical background with patient management
Medical background in industry
Primary care background
EDUCATION:
MD or DO ONLY
PREFERRED FIELD OF STUDY:
3-5 years clinical/medical affairs experience in life science field, business development experience desired
Director, Clinical Due Diligence
SUMMARY:
Reports to the Chief Medical Officer, the Director of Clinical Due Diligence is charged with onsite and offsite review of clinical opportunities in collaboration with business development. Individual is intended to work with business teams in evaluating potential business deals from medical and clinical research perspective. Will be required to meet and counsel executive leadership.
RESPONSIBILITIES:
Provides business development leadership team medical and clinical due diligence of candidate early development to post-marketed products
Travel with team for due diligence of business licensing candidates
Working knowledge of pharmacovigilance and risk management activities
Participate in product development meetings
Prepare/deliver presentations on medical perspective
Evaluate in-license pharmaceutical candidates
Assess qualitative and quantitative composition of in-vitro and in-vivo product performance
Attend professional conferences and meetings
REQUIREMENTS:
Understand clinical development of pharmaceutical drug products, modeling and population PK analyses
Excellent interpersonal skills, self-motivation, and positive attitude
Analytical skills as well as excellence in oral and written communications
Ability to review business development projects
Have experience in medical affairs and clinical research
Ability to handle multiple issues on multiple projects simultaneously.
Ability to maintain a high degree of independence with respect to decision making and problem solving
Liaise with other departments/ divisions to ensure successful outcome in due diligence of projects
Strong negotiating skills
Must have ability to analyze and evaluate processes and procedures
Previous experience in business development
Clinical background with patient management
Medical background in industry
Primary care background
EDUCATION:
MD or DO ONLY
PREFERRED FIELD OF STUDY:
3-5 years clinical/medical affairs experience in life science field, business development experience desired
Contact: Britt Kelley
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