Job Description

• Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
• We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description

Job Description

:
The Fact Checker (Medical Writer III) works closely with Medical Writers to confirm that supplied references adequately support claims being made in pharmaceutical advertising materials for US and global audiences. The Fact Checker verifies medical and other data and creates annotated reference documents that show where claims are in published sources to facilitate Veeva PromoMats project submission and Medical/Regulatory/Legal review.
Job Responsibilities:

• Checks claims in advertising and promotional documents against published sources before projects are submitted for Medical/Regulatory/Legal review.
• Ensures that suitable references are used to support all product and promotional claims in text, graphs, charts, tables, and statistical analyses.
• Creates annotated documents to be used for submitting/linking projects in Veeva PromoMats.
• Works with writers, editors, account managers, and Veeva submission specialist to ensure project submissions are accurate, current, and compliant.
• May be asked to research promotional claims and perform data mining, working with Clinical Study Reports (CSRs) and resources from the client Library.
• Organizes and manages approved references on the A3 server.
• Links claims to published sources in Veeva PromoMats, as needed.

Requirements:

• Bachelor’s degree or higher (in a medical-related field a plus [eg, biology or chemistry])
  or equivalent experience within the pharmaceutical or related industry.
• 3+ years of medical fact checking experience.
• Proven ability to research, understand, and interpret medical and scientific data.
• Working knowledge of regulations and standards related to promotion of pharmaceutical products and AMA style guidelines.
• Proficiency in Adobe Acrobat Pro and MS Word; familiarity with the Veeva PromoMats platform a definite plus.
• Ability to work in fast-paced environment and juggle multiple deadlines, without sacrificing quality or accuracy.
• Analytical thinker and proactive problem solver.
• Ability to work independently and collaborate with team members, as needed.
• Advanced written, verbal, time management, and organizational skills.

Additional Information

All your information will be kept confidential according to EEO guidelines.

Job Tags

Contract work, Immediate start,

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