Medical Affairs Communications – Womens Health Position Available In Morris, New Jersey

job summary: The Medical Affairs Communications and Publication Contractor will support all Medical Affairs Communications and Publication functions within WHC. The contractor is responsible for providing accurate, timely, unbiased, and up to date medical & scientific information to internal and external customers. The incumbent carries out this role in accordance with departmental SOPs, company corporate policy, and other legal & regulatory requirements. The incumbent will work in close collaboration with global and country medical affairs and cross-functional colleagues, ensuring accurate and compliant scientific information is delivered to internal and external customers.

location:

Whippany, New Jersey job type: Contract salary: $69.17 – 81.37 per hour work hours: 9 to 5 education: Doctorate responsibilities: The primary responsibilities of this role: Respond to verbal, written, and electronic medical/product inquiries from Healthcare Professionals, (e.g., Physicians, Pharmacists, Nurses), Consumers, accounts, Insurance and Government personnel that have been escalated from Customer Care Services (Call Center)Perform QA on the call center responses to HCPs to ensure accurate and compliant responses are being providedDirect or participate in the approval process for custom and standard inquiry responsesReview all standard responses within the therapeutic area of responsibility for accuracy, relevance, and timeliness prior to final approval by the Med Comm Director or Senior DirectorGuide Medical Information personnel such that accurate and up to date information are provided to external customers and supervises and facilitates the search, review and interpretation of medical and scientific dataPrepare and share Medical Information and PIR inquiries report for broader Medical Affairs team to guide Medical Affairs and MSL strategySupport the Med Communications and Publication lead in preparation of Publication workshop to create publication strategy for WHC portfolioSupport the Med Communications and Publication lead in the execution of publications plan, including tracking timelines, coordinating with authors and agencies, and ensuring deliverable align with scientific and strategic objectivesParticipate and assist Med Communications and Publication Director in the Medical review and approval of all Advertising & Promotion and Sales Training materials. Medical Affairs representative for LMR (Legal, Medical, Regulatory) team for assigned products and or therapeutic areaReview the scientific literature to develop content for new Medical Content standard letters and FAQs and revisions of existing letters for a company disease state area combining clinical experience with critical analysis of clinical literature to synthesize an appropriate solution to a customer specific, drug related problem while keeping within legal and regulatory guidelinesActively participate in marketing brand product teams, communications committees, product advisory board meetings, and other company meetings to ensure that the MC scientifically accurate public health message supports business unit goals and is aligned to promotional materials and campaignsChampion regular meetings with Medical Affairs (Medical Affairs, HEOR, MSLs,) and other business partners (Safety, Product Quality Complaints, Sales, Sales Training, Marketing) to ensure the safe and appropriate use of company products assuring public health oriented responses and to assure the key medical messages are consistent and accurate throughout the companyPlan and Manage the Medical Affairs booth for company products at Medical and Scientific conventions and conferences qualifications:

Required Qualifications:

Healthcare Professional (PharmD, PhD, MD) with experience within a pharmaceutical or medical device company; or equivalent clinical experience required.

Experience in a formal drug information center or equivalent clinical experience required.

Excellent oral and written communication skills are required. Knowledge of FDA regulations regarding the dissemination of Medical Information, drug promotion and adverse event and product quality complaint reporting is required;Computer proficiency required;Proven track record of successfully implementing scientific communication projects at the Senior Manager level.

Preferred Qualifications:

2+ years of industry experience, preferred.

skills:

FDA, Medical Publications Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate’s education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. job detailssummary$69.17 – $81.37 per hourcontractpostgraduate degreecategorylife, physical, and social science occupationsreference51067job details job summary: The Medical Affairs Communications and Publication Contractor will support all Medical Affairs Communications and Publication functions within WHC. The contractor is responsible for providing accurate, timely, unbiased, and up to date medical & scientific information to internal and external customers. The incumbent carries out this role in accordance with departmental SOPs, company corporate policy, and other legal & regulatory requirements. The incumbent will work in close collaboration with global and country medical affairs and cross-functional colleagues, ensuring accurate and compliant scientific information is delivered to internal and external customers.

location:

Whippany, New Jersey job type: Contract salary: $69.17 – 81.37 per hour work hours: 9 to 5 education: Doctorate responsibilities: The primary responsibilities of this role: Respond to verbal, written, and electronic medical/product inquiries from Healthcare Professionals, (e.g., Physicians, Pharmacists, Nurses), Consumers, accounts, Insurance and Government personnel that have been escalated from Customer Care Services (Call Center)Perform QA on the call center responses to HCPs to ensure accurate and compliant responses are being providedDirect or participate in the approval process for custom and standard inquiry responsesReview all standard responses within the therapeutic area of responsibility for accuracy, relevance, and timeliness prior to final approval by the Med Comm Director or Senior DirectorGuide Medical Information personnel such that accurate and up to date information are provided to external customers and supervises and facilitates the search, review and interpretation of medical and scientific dataPrepare and share Medical Information and PIR inquiries report for broader Medical Affairs team to guide Medical Affairs and MSL strategySupport the Med Communications and Publication lead in preparation of Publication workshop to create publication strategy for WHC portfolioSupport the Med Communications and Publication lead in the execution of publications plan, including tracking timelines, coordinating with authors and agencies, and ensuring deliverable align with scientific and strategic objectivesParticipate and assist Med Communications and Publication Director in the Medical review and approval of all Advertising & Promotion and Sales Training materials. Medical Affairs representative for LMR (Legal, Medical, Regulatory) team for assigned products and or therapeutic areaReview the scientific literature to develop content for new Medical Content standard letters and FAQs and revisions of existing letters for a company disease state area combining clinical experience with critical analysis of clinical literature to synthesize an appropriate solution to a customer specific, drug related problem while keeping within legal and regulatory guidelinesActively participate in marketing brand product teams, communications committees, product advisory board meetings, and other company meetings to ensure that the MC scientifically accurate public health message supports business unit goals and is aligned to promotional materials and campaignsChampion regular meetings with Medical Affairs (Medical Affairs, HEOR, MSLs,) and other business partners (Safety, Product Quality Complaints, Sales, Sales Training, Marketing) to ensure the safe and appropriate use of company products assuring public health oriented responses and to assure the key medical messages are consistent and accurate throughout the companyPlan and Manage the Medical Affairs booth for company products at Medical and Scientific conventions and conferences qualifications:

Required Qualifications:

Healthcare Professional (PharmD, PhD, MD) with experience within a pharmaceutical or medical device company; or equivalent clinical experience required.

Experience in a formal drug information center or equivalent clinical experience required.

Excellent oral and written communication skills are required. Knowledge of FDA regulations regarding the dissemination of Medical Information, drug promotion and adverse event and product quality complaint reporting is required;Computer proficiency required;Proven track record of successfully implementing scientific communication projects at the Senior Manager level.

Preferred Qualifications:

2+ years of industry experience, preferred.

skills:

FDA, Medical Publications Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate’s education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.