Life science jobs in India

Senior Manager - Secretarial & Legal. Minimum 10 years post qualification work experience in corporate secretarial Company Law and SEBI related compliances. Hands on experience in uploading files on MCA NSE BSE CDSL and NSDL portal. · ...

A Senior Manager - Secretarial & Legal is required for a listed entity in the pharmaceutical sector. · ...

The Life Sciences Domain SME provides deep expertise and strategic guidance in areas such as pharmaceuticals, · biotechnology, clinical research, · regulatory affairs, · and life-science business processes.Serve as the primary subject matter expert in life sciences · (pharma, bio ...

We are looking for a detail-oriented Purchasing Associate/accountable AP/Procurement Specialist to manage vendor payments, procurement records, · and basic accounting operations. · Handle billing,payments,and settlements related to procurementAccurately record Purchase Orders (PO ...

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 for regula ...

We are looking for a detail-oriented Purchasing Associate to manage vendor payments and procurement records. The role plays a key part in ensuring smooth cash flow and accurate records. · Degree in Accounting Finance Business Administration B.Com preferred · Minimum 2 years of ex ...

Outpace Consulting Services is seeking 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 ...

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 re ...

Graduate or post graduate in Pharmacy, Nursing or life sciences. · Certification in Medical writing or Diploma in clinical research would be desirable. · Preferred experience for the Author role: · Preferably 1 to 2 years of experience in medical writing domain. · Life science gr ...

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 datasets ...

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 review · ...

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 ...

Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process · Create edit check specifications and program or modify checks at study level within EDC · Setup different instances of study URL (e.g.: UAT (User Acceptance Testing) ...

Job Overview: · The Medical Reviewer is responsible for the evaluation and analysis of clinical data to ensure accuracy, compliance with regulations, and the highest quality standards. This role involves reviewing clinical trial data, medical documentation, and regulatory submiss ...

Minimum 2 years of experience for Senior Statistical programming is a mandate. · Having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards. · Associate should be able to manage communication with customers, track and ensur ...

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 ...

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 in su ...

Minimum 2 years of experience for Senior Statistical programming is a mandate. · Having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards. · Associate should be able to manage communication with customers, track and ensur ...

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 client ...

1. Data validation test script creation: · Create necessary validation scenarios needed to ensure checks are functioning as required and document scenarios in the Data Validation Specification(DVS). Document expected results for each testing scenario. · Feedback to the clinical D ...