Medical Writer I
Medical Writer I
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Job Description
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
Job Description Summary :
Responsible for management of scheduled and unscheduled aggregate reports including but not limited to Periodic Safety Reports (PSRs) including Periodic Safety Update Reports (PSURs) Periodic BenefitRisk Evaluation Reports (PBRERs) Addendum to Clinical Overviews (ACOs) SemiAnnual Safety Reports (SASRs) Corporate Addendum Reports United States Periodic Adverse Drug Experience Reports (PADERs) Development Safety Update Reports (DSURs) Annual RiskBenefit Evaluation (ARBE) report Risk Management Plan (RMP) Safety statements Health Hazard Evaluation (HHE) Drug Safety Report (DSR) Clinical Overview (CO) Safety Evaluation Report (SER) Investigational New Drug Annual Report (INDARs) as well as preparing document of comparison between local and global labeling document (if applicable) and checking of International Nonproprietary names (INNs) for inclusion in a PSR as per client requirements and signal detection and management (where applicable).
Generating Line Listings creating drug lists/drug folders performing regulatory submissions tests electronic submissions gateways and tracking compliance monitoring of submissions in accordance with client/international conventions
Responsible for preparing the narratives associated with the clients/sponsors products from clinical trials for Clinical Study Reports (CSRs) or in order to support any health authority requests in accordance with regulatory and clients/sponsors requirements
Scheduling and Attending meetings/ Drafting meeting agenda and minutes/Tracking action items.
Job Description:
- Preparing/updating/merging RMPs/Company CoreRMPs (CCRMPs) preparing a health authority response document along with RMS update in accordance with client requirements/conventions and SOPs.
- Managing scheduled and unscheduled aggregate reports including but not limited to Periodic Safety Update Reports (PSURs) Periodic Benefit Risk Evaluation Reports (PBRERs) Addendum to Clinical Overviews (ACOs) SemiAnnual Safety Reports (SASRs) Corporate Addendum Reports United States Periodic Adverse Drug Experience Reports (PADERs) Development Safety Update Reports (DSURs) Annual RiskBenefit Evaluation (ARBE) report Safety statements Health Hazard Evaluation (HHE) Drug Safety Report (DSR) Clinical Overview (CO) Safety Evaluation Report (SER) Investigational New Drug Annual Report (INDARs) comparison document between local and global labeling document (if applicable)and checking of International Nonproprietary names (INNs) for inclusion in a PSR as per client requirements and conventions and SOPs
- Conducting critical appraisal and systematic review of literature with a focus on background epidemiology specifically information on the incidence prevalence and risk factor in patient populations for inclusion in drug Safety Reports and RMPs
- Providing input and developing literature search strategies for the epidemiology section of safety reports
- Applying epidemiological methods and calculations to data available in literature to support the background rates of the issues under evaluation for the safety reports
- Generating Line Listings for submissions/ to identifying discrepancies and ensuring resolution of the discrepancies
- Revising document drafts based on the review comments from team members to ensure inclusion of all relevant input.
- Ensuring that all work is complete and of high quality prior to team or client distribution. Confirm data consistency and integrity across the document.
- Performing aggregate report compliance activities including quality review to check the data/facts and internal consistency across various type of aggregate reports including but not limited to PBRERs Ad hocs HHEs LJDs tables RMP Pharmacovigilance System Master File (PSMF) document (as applicable).
- Distributing of final reports to the stakeholders including partners affiliates and submission to health authorities according to the agreed timelines distribution lists and email templates (as required).
- Scheduling and Attending meetings/ Drafting meeting agenda and minutes/Tracking action items.
Employment Type
Full-Time
