Pharma Jobs

  Medical Writer Aabhineos Customs Pune, Maharashtra, India  Posted 1 day ago Save Save   Easy apply Job description Required Freelance professional medical content writer/reviewer/editor. Expertise in writing clear, concise, comprehensible, and coherent content in the field of Health and Medical Sciences. Specialised in Botany, Zoology or Human Biology.

  Medical Writer (cer) MAKRO Hyderabad, IN Posted 1 day ago Save Save   Apply Job description MakroCare is an Expert Strategic Development andCommercialization Global Partner for Pharmaceutical Biotechnology and MedicalDevice industries Our Experience Programs and Processes bring a New Dimensionto Development Strategy Regulatory Risk Planning Management ClinicalResearch Medical Scientific Support and Emerging Region Expansion Medical Writer CER 1 A CER writer will have an in-depth knowledge ofmedical writing and will be responsible for developing Clinical EvaluationReports CERs and assessing the need for product change CERs 2 This individual will have demonstrated expertise inpartnering

  Medical Writer PPD Delhi, IN Posted 18 hours ago Save Save    work here Job description Job Description The Medical Writer researches, prepares, and coordinates scientific publications. The Medical Writer is responsible for researching, writing, and editing clinical/statistical reports and study protocols, and summarizing data from clinical studies for submission to the Food and Drug Administration (FDA).The Medical Writer researches, prepares, and coordinates scientific publications. The Medical Writer is responsible for researching, writing, and editing clinical/statistical reports and study protocols, and summarizing data from clinical studies for submission to the Food and Drug Administration (FDA). Job Qualification Education And Experience BS/BA in a scientific discipline(or licensed certification) with 4+ years relevant writing experience  or Advanced degree with 2+ years relevant writing experience 2 years relevant experience as a medical writer, preferably...

  42088 - Medical Writer 2 IQVIA Thane, Maharashtra 42088 - Medical Writer 2 IQVIA - Thane, Maharashtra Qualifications Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field (Required); Req Master's Degree Master's Degree in life sciences related discipline or related field (Pref); Pref Ph.D. Ph.D. in life sciences related discipline or related field (Pref); Pref Typically requires at least 3 years of prior relevant experience and related competency levels. Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.; Ability to identify deficiencies, errors, and inconsistencies in a protocol or report.; Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.; Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output. Ability to integrate, interp...

        SYNGENE Hiring Career Opportunities: Junior Manager - Medical Writing Apply Now SYNGENE Hiring Career Opportunities: Junior Manager - Medical Writing Apply Now Job Purpose: To help in preparation of clinical trial related documents like synopsis, protocol, Risk Evaluation and Mitigation Strategies (REMS), Informed Consent Document (ICD), Clinical Study Report (CSR), Common Technical Document (CTD), electronic CTD (eCTD) modules and any other document as needed for regulatory submission/requested by sponsor Key Responsibilities: •    Independently develop and finalize clinical and scientific documents such as (but not limited to) synopses, protocols, investigator brochures, Clinical Study Reports (CSRs), Informed Consent Documents (ICDs), relevant regulatory documents and clinical documents, Electronic Common Technical Document (eCTD) modules, etc. covering various therapeutic areas and all phases of clinical research •   ...

Staff Clinical Science / Medical Writing KritiKal Solutions Delhi, IN Posted 21 hours ago Save Save   Apply Job description Author clinical trial protocols, interim and final clinical study reports,including Clinical Evaluation Plans and reports, PMCF Plans and reports, summary of effectiveness and safety integrated safety/performance data summaries Perform formal literature searches, and succinctly summarize scientific content for assigned projects. Contribute to Pre-Submissions, Design and Value dossiers for matrix submissions Contribute to Publications in drafting abstracts, podium presentations and manuscripts Provide clinical science subject matter expertise and consultation to Clinical Research Associates, Biostatistics, Data Management, Regulatory Affairs, Clinical Safety and other internal and external stakeholders. Collaborate with other staff to resolve complex or unclear situations. Propose and participate in departmental continuous improvement initiatives. Assist in tra...