Life science jobs in Navi Mumbai

 ...Assessment findings   Educational Qualification • Education: Science/Engineering Graduate/Post- Graduate • Work Experience: Overall...  ...01:2015, ISO 13485 and other applicable governing regulations in Life Science domain. • Good knowledge of standards / accreditations... 

Role & responsibilities: Candidate should have 2-5 years of experience of CDM with experience in Conduct Scope of work Perform day-to-day Clinical Data Management activities. Experience in doing external data reconciliation Work and coordinate with the team to perform...

 ...Outpace Consulting Services is seeking a Regulatory Medical Writer with expertise in Life Sciences for a leading ITES company. In this role, you'll be responsible for developing clear, accurate, and well-structured medical and scientific documents specifically tailored... 

 ...an Aggregate Report Writer specializing in Pharmacovigilance (PV) Aggregate SUSAR Reporting for a leading ITES company in the Life Sciences domain. In this role, you will be responsible for the end-to-end process of preparing, writing, and reviewing complex periodic aggregate... 

 ...Outpace Consulting Services is seeking a Medical Writer specializing in Life Sciences and Clinical Studies for a leading ITES company. This role is responsible for developing clear, accurate, and well-structured medical and scientific documents for various audiences, including... 

Role & responsibilities: 1.Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. 2. Develop library of reusable checks working closely with data engineers and config...

 ...Outpace Consulting Services is seeking a talented Clinical SAS + SQL Programmer with expertise in Life Sciences for a leading ITES company. This role is crucial for statistical programming within the clinical domain, focusing on the development and validation of analysis... 

 ...Outpace Consulting Services is looking for an experienced Lead Data Manager in the Life Sciences domain for a leading ITES company. In this role, you will lead daily Clinical Data Management (CDM) activities, ensuring the delivery of high-quality, error-free databases... 

Build and process submission dossiers of low-to-moderate complexity: Submission Dossiers that may be periodic (e.g.: safety reports) or minor amendments (e.g.: IND Amendment, DMF Amendment, CMC Update as appropriate to level, etc) or otherwise not major applications but...

# Author a company clinical comment (CCC) for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). # Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. # Perform the following...

Role & responsibilities: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) To perform all pre-DLP activities and planning for all assigned reports as per...

Programming, specifically J Review, SQL, R and GitHub. Good to have Python. • Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. • Develop library of reusable ...

1. Develop documents e.g. Clinical Trial Protocol (CTP) Trial Statistical Analysis Plan (TSAP) Randomization specifications & initiate randomization scheme creation Participate in the development of Integrated Quality and Risk Management (IQRM) plan and MQRP 2. Support...

Job Description: Active involvement in CAPA management activities within the team. Preferably must have faced Internal /Client audit. Working knowledge of the global pharmaceutical/pharmacovigilance regulations (ICH/ Good Pharmacovigilance modules) is preferable. ...

 ...Outpace Consulting Services is seeking a skilled Clinical SAS + SQL Programmer for a leading ITES company in the Life Sciences domain. This role is central to Clinical Data Management, focusing on developing and applying programming expertise to ensure high-quality databases... 

Create data cleaning reporting solutions, study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. Contribute to process improvements and development of programming standards using R. Minimum of 3 years...

Review protocol and provide suggestions Respond to queries/ clarifications from EC/ IRBs Answer medical questions from sites or project team Respond to queries from sites with regard to protocol Attend drug safety meetings/ external meetings Patient eligibility...

 ...performing tasks such as communication with the appropriate Clinical Safety Personnel and where appropriate with the Clinical Science Group ensuring that all necessary queries have been addressed. Accountable for confirming that the correct strategy has been taken... 

 ...abysmal. Their chances of attending college, or building a career are significantly lower than their high-income peers, condemning them to a life without voice or choice. iTeach was born in 2015 to challenge this status quo and create a level playing field for ALL children.  We... 

 ...efficient model lifecycle managementSkillset Requirements : Technical Lead (Mandatory) :- 5- 10 years of relevant experience in data science- Minimum 5 years of experience in Python programming- At least 3 years of experience in machine learning and NLP- Minimum 2 years of...