Syneos Medical Writer Job For Life Sciences Candidates, Apply Online
Syneos Medical Writer Job For Life Sciences Candidates, Apply Online. Syneos Health Life Sciences vacancy is available. Interested and eligible applicants can check out all of the details on the same below
Designation – Medical Writer II
Job Location – India-Asia Pacific – IND-Gurugram-PresidencyTwrsMGr
Job ID – 22009060
Description
Job Responsibilities
- Works cross-functionally and collaboratively to plan and coordinate the global transparency activities (posting of the protocol registration form and summary results on clinicaltrials.gov, EudraCT, and similar databases worldwide, Lay Summaries of results for Patients and the general public, Clinical Data Sharing, and other transparency-related activities in the EU, US and third countries) and to ensure/support compliance with procedures and to manage external communication
- Ensuring the development of high-quality registration, maintenance, and results in deliverables that are compliant with all applicable policies, procedures, and regulations
- Undertakes project-specific activities at high quality and in defined timelines according to standard processes and operating procedures
- Systematically perform quality control checks of documents prepared by colleagues against a pre-specified checklist generated in the project or SOP
- Maintain accurate and up-to-date records of individual study activities for timeline integrity, compliance, and relevant metrics tracking
- Perform detailed analyses on a planned and ad hoc basis, relating to processes and their outputs
- Ensure to abide by the Client process
- Completion of Internal and Client specific training
Qualifications
What we’re looking for
- Educational qualifications: A minimum of a scientific graduate degree in life sciences.
- Good knowledge of regulatory requirements or guidance pertaining to the service line.
- Good understanding of clinical development processes including principles of clinical study operations and ICH-GCP guidelines. Clear written and verbal communication skills
- Good knowledge of basic computer applications, e.g. MS Word/ PowerPoint/ Excel, will be required.
- A person should understand & comprehend protocol and clinical study reports from a disclosure perspective.
- Good understanding of clinical trial disclosure fundamental
- Core competencies for this role include the ability to demonstrate:
- Analytical capabilities with scientific and clinical data.
- Professional working environment
- Ownership of the work allocated
- Commitment to highest quality outputs, including high attention to detail
- Enthusiasm and pro-activity
- Effective team working
- Ability to build rapport/ relationships with project-specific client colleagues.
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