Medical Monitor (MUST HAVES: patient safety, pharmacovigilance, and post-marketing medical sensitivity assessments & medicine and pharmaceutical product, preferably across multiple therapeutic areas)

JOB TITLE: Medical MonitorLocation: Lawrence Township, NJ (100% onsite)Duration: 6 months initial (potential extension/potential right to hire)

Job Description: Position Summary:• The Established Brands medical scientist-contractor is responsible for the medical oversight of activities for brands in late stages of life cycle and those which have undergone Loss-of-ExclusivityKey Responsibilities:• Lead medical input for brand cross-functional teams for assigned products.• Provide medical input to patient safety monitoring of the brand and available literature findings, propose labeling recommendations based on signal detection activities and pharmacovigilance findings.• Provide Medical Assessments of Risk/Benefit of assigned products regarding new indications, safety or stability issues, medical necessity/sensitivity assessments or other actions that require reappraisal of the product Risk/Benefit.• Provide medical input for regulatory requirements, including Response to Health Authorities queries and support for registration renewals and label periodic reviews.• Provide medical support to the Company Core Data Sheet content review and development.• Provide medical evaluation and appropriate communications to additional documents and activities such as: Dear Health Care Professional letters, Clinical Overview for Type II variation, Periodic Benefit-Risk Evaluation regulatory document submissions and coordinate expert reports.• Compliance Support delivery of medical affairs compliance needs for the assigned portfolio as appropriate.Position Competencies:• Demonstrate ability to apply Client operating philosophy, company shared values and operate within company policies and procedures and appropriate regulations.• Strong ability to operate effectively within highly matrixed and collaborative environment:o Partner with local market organizations as appropriate for medical deliverables and portfolio functions.o Collaborate with key cross-functional partners, Global Regulatory, Global Labeling, Patient Safety, Quality & Compliance.• Knowledgeable and skilled in medicine and pharmaceutical product preferably with experience in pharmaceutical industry and post-marketing safety.• Ability to provide input to cross-disciplinary matrix teams, promote collegiality and teamwork among team members.• Ability to think clearly and decisively and present independent, reasoned solutions to identified safety issues.• Familiarity with regulatory guidelines.• Excellent oral and written communication, interpersonal and time management skills.• Demonstrate flexibility, open mindedness and adaptability in a rapidly changing environment.

Qualifications:• MD or Equivalent required• Board certification and medical specialty highly preferred• 2-4+ years in clinical practice• 1-2+ years of pharmaceutical industry experience required with 5+ years preferred• 1-2+ years of clinical safety experience strongly preferred, with experience with pharmacovigilance-safety• Experience in multi-brand experience would be an advantage.

If you feel you are qualified with the required skills and if you are interested, please free to send your word version most updated resume TAILORED to the job description above to June@eclaro.com or call (212)804-7476. If hired, you will enjoy the following Eclaro Benefits:401k Retirement Savings Plan administered by Merrill LynchCommuter Check Pretax Commuter BenefitsEligibility to purchase Medical, Dental & Vision Insurance through Eclaro Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.