Pharmacovigilance Physician
Position Summary
The Pharmacovigilance Physician is a medical physician (MD DO or equivalent) who has the scientific clinical and therapeutic area expertise responsibility for medical review of individual case safety reports (ICSR) to determine benefit-risk analysis and provide medical assessment statements review and analyze aggregate data sets from internal or external sources for benefit-risk assessments review and interpretation of clinical and post marketing data for the purpose of signal detection evaluation verification and participation in safety meetings with clients. The physician will also assist in drafting reviewing and refining medical-content intensive portions of periodic safety reports (PADERs PSURs DSURs PBRERs IND Annual Reports) Investigators Brochure (IB) updates Clinical Safety Summaries (ISS) US and international product labeling documents and ad hoc safety information requests from regulatory authorities. This position is also responsible as required for drafting reviewing and refining risk management plans and risk evaluation and mitigation strategies for the client. The Pharmacovigilance Physician will assist and support the Qualified Person for Pharmacovigilance as required.
Essential Functions
To perform this job successfully an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
Essential Functions Statements:
- Accountable for medical evaluation and interpretation of aggregate safety information for periodic reports safety signal detection activities and ad-hoc information requests.
- Accountable for risk-benefit analysis and assessment for client products per client contract.
- Lead and participate in safety meetings with clients.
- Support the pharmacovigilance system for Med Communications and for each client per client contract.
- Integrate knowledge of regulations and compliance guidelines to ensure compliance of medical assessment activities.
- Provide expertise and/or represent the client for interactions with safety monitoring boards and/or regulatory authorities.
- Support the Qualified Person for Pharmacovigilance as required per client contract.
- Other pharmacovigilance activities as requested.
POSITION QUALIFICATIONS
Licensed medical physician in good-standing in the state(s) of licensure (MD DO etc.) plus one (1) year pharmacovigilance experience or other equivalent experience. Or Unlicensed medical physician (MD DO etc.) with no record of past or present Medical Board disciplinary action; plus ten (10) years of combined pharmacovigilance experience clinical healthcare provider experience or other equivalent experience.
Competency Statements
Self-Motivated - Ability to be internally inspired to perform a task to the best of ones ability using his or her own drive or initiative.
Organized - Possessing the trait of being organized or following a systematic method of performing a task.
SKILLS AND ABILITIES
Education: Licensed medical physician in good-standing in the state(s) of licensure (MD DO etc.). Prefer board certification in related area for client being supported. Epidemiology degree is a plus.
Experience: One year related pharmacovigilance experience in the pharmaceutical industry or other equivalent experience such as clinical trial investigator health authority inspector epidemiologist etc.
Computer Skills: Prefer proficiency with Microsoft Office and content management systems.
Other Requirements: Understanding of legal regulatory and compliance requirements with regards to pharmacovigilance based on global regulations for EU FDA Japan MHLW UK MHRA and other entities and ICH guidelines.
Work Environment
Remote: Romania / Poland or Portugal
The company has reviewed this job description to ensure that essential functions and basic duties have been included. It is intended to provide guidelines for job expectations and the employees ability to perform the position described. It is not intended to be construed as an exhaustive list of all functions responsibilities skills and abilities. Additional functions and requirements may be assigned by supervisors as deemed appropriate. This document does not represent a contract of employment and the company reserves the right to change this job description and/or assign tasks for the employee to perform as the company may deem appropriate.
Disclaimer
By attaching your Curriculum Vitae (CV) resume and/or completing an online application you are consenting to the collection processing use transfer (including but not limited to other countries/jurisdictions) storage and disclosure of your personal data as described in the Med Communications Inc. Privacy Policy. Please read this policy carefully for more information on your rights regarding personal data protection.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race color religion sex national origin age disability genetic information or veteran status.
Recruitment Agency Notice:
Thank you for your interest in working with Med Communications. We kindly ask that recruitment agencies avoid sending unsolicited CVs as our in-house team manages all hiring processes.
Please be aware that any unsolicited CVs or candidate profiles received without prior engagement or agreement with our recruitment team will be considered free and carry no obligation on the part of Med Communications. We thank you for your compliance with our policy.
Should collaboration opportunities arise we will reach out to preferred partners proactively. Your understanding and cooperation are appreciated.
Pharmacovigilance PhysicianPosition Summary The Pharmacovigilance Physician is a medical physician (MD DO or equivalent) who has the scientific clinical and therapeutic area expertise responsibility for medical review of individual case safety reports (ICSR) to determine benefit-risk analysis and p...
Pharmacovigilance Physician
Position Summary
The Pharmacovigilance Physician is a medical physician (MD DO or equivalent) who has the scientific clinical and therapeutic area expertise responsibility for medical review of individual case safety reports (ICSR) to determine benefit-risk analysis and provide medical assessment statements review and analyze aggregate data sets from internal or external sources for benefit-risk assessments review and interpretation of clinical and post marketing data for the purpose of signal detection evaluation verification and participation in safety meetings with clients. The physician will also assist in drafting reviewing and refining medical-content intensive portions of periodic safety reports (PADERs PSURs DSURs PBRERs IND Annual Reports) Investigators Brochure (IB) updates Clinical Safety Summaries (ISS) US and international product labeling documents and ad hoc safety information requests from regulatory authorities. This position is also responsible as required for drafting reviewing and refining risk management plans and risk evaluation and mitigation strategies for the client. The Pharmacovigilance Physician will assist and support the Qualified Person for Pharmacovigilance as required.
Essential Functions
To perform this job successfully an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
Essential Functions Statements:
- Accountable for medical evaluation and interpretation of aggregate safety information for periodic reports safety signal detection activities and ad-hoc information requests.
- Accountable for risk-benefit analysis and assessment for client products per client contract.
- Lead and participate in safety meetings with clients.
- Support the pharmacovigilance system for Med Communications and for each client per client contract.
- Integrate knowledge of regulations and compliance guidelines to ensure compliance of medical assessment activities.
- Provide expertise and/or represent the client for interactions with safety monitoring boards and/or regulatory authorities.
- Support the Qualified Person for Pharmacovigilance as required per client contract.
- Other pharmacovigilance activities as requested.
POSITION QUALIFICATIONS
Licensed medical physician in good-standing in the state(s) of licensure (MD DO etc.) plus one (1) year pharmacovigilance experience or other equivalent experience. Or Unlicensed medical physician (MD DO etc.) with no record of past or present Medical Board disciplinary action; plus ten (10) years of combined pharmacovigilance experience clinical healthcare provider experience or other equivalent experience.
Competency Statements
Self-Motivated - Ability to be internally inspired to perform a task to the best of ones ability using his or her own drive or initiative.
Organized - Possessing the trait of being organized or following a systematic method of performing a task.
SKILLS AND ABILITIES
Education: Licensed medical physician in good-standing in the state(s) of licensure (MD DO etc.). Prefer board certification in related area for client being supported. Epidemiology degree is a plus.
Experience: One year related pharmacovigilance experience in the pharmaceutical industry or other equivalent experience such as clinical trial investigator health authority inspector epidemiologist etc.
Computer Skills: Prefer proficiency with Microsoft Office and content management systems.
Other Requirements: Understanding of legal regulatory and compliance requirements with regards to pharmacovigilance based on global regulations for EU FDA Japan MHLW UK MHRA and other entities and ICH guidelines.
Work Environment
Remote: Romania / Poland or Portugal
The company has reviewed this job description to ensure that essential functions and basic duties have been included. It is intended to provide guidelines for job expectations and the employees ability to perform the position described. It is not intended to be construed as an exhaustive list of all functions responsibilities skills and abilities. Additional functions and requirements may be assigned by supervisors as deemed appropriate. This document does not represent a contract of employment and the company reserves the right to change this job description and/or assign tasks for the employee to perform as the company may deem appropriate.
Disclaimer
By attaching your Curriculum Vitae (CV) resume and/or completing an online application you are consenting to the collection processing use transfer (including but not limited to other countries/jurisdictions) storage and disclosure of your personal data as described in the Med Communications Inc. Privacy Policy. Please read this policy carefully for more information on your rights regarding personal data protection.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race color religion sex national origin age disability genetic information or veteran status.
Recruitment Agency Notice:
Thank you for your interest in working with Med Communications. We kindly ask that recruitment agencies avoid sending unsolicited CVs as our in-house team manages all hiring processes.
Please be aware that any unsolicited CVs or candidate profiles received without prior engagement or agreement with our recruitment team will be considered free and carry no obligation on the part of Med Communications. We thank you for your compliance with our policy.
Should collaboration opportunities arise we will reach out to preferred partners proactively. Your understanding and cooperation are appreciated.
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