Senior Clinical Regulatory Document Manager

About the RoleAt TransPerfect, we are seeking a skilled Regulatory Publishing Specialist to join our team. This exciting opportunity will see you play a key role in publishing clinical study reports, IND documents, and other regulatory materials according to ICH and eCTD standards.

Job Summary:We are seeking detail-oriented and organized individuals to join our team as Clinical Research Coordinators. Candidates with minimum 1-3 years experience in clinical trials need only apply.Key Responsibilities:Study Coordination: Assist in the planning, initiation, and coordination of clinical trials under the supervision of the Principal...

We are seeking a highly skilled Regulatory Project Manager to join our team at ProductLife Group. As a key member of our clinical trials department, you will be responsible for managing projects from initial preparation to final submission and notification of results. Your expertise in regulatory affairs and clinical trials management will ensure seamless...

About the RoleAs a Senior Clinical Trial Acceleration Manager at Bristol Myers Squibb, you will play a pivotal role in managing and executing centralized activities in support of global trials with an emphasis on clinical documentation.Key Responsibilities:Manage performance and career development of Senior Document Coordinators and Document...

**Job Summary:**We are seeking a skilled Senior Regulatory Publisher to join our team at TransPerfect. This is an exciting opportunity to work with Regulatory Affairs and publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards.About the Role:The...

Job Title:Senior Clinical Data Analyst - R ProgrammerAbout the Role:We are seeking a highly skilled Senior Clinical Data Analyst with expertise in R programming to join our team at Trigent Software Inc. As a key member of our data management team, you will be responsible for developing and maintaining programs using R to generate Tables, Listings, and...

About the Role:We are seeking a highly skilled Clinical Documentation Specialist to join our team at Heart Vascular and Leg Center. This is a unique opportunity to utilize your clinical documentation expertise in a remote setting, working closely with US-based healthcare providers.As a Clinical Documentation Specialist, you will play a crucial role in...

About UsNaari Pharma Pvt Ltd. is a leading pharmaceutical company dedicated to delivering innovative solutions in the field of clinical studies.Job DescriptionWe are seeking an experienced Senior Project Manager to oversee the coordination of BA/BE and clinical studies. The successful candidate will have a proven track record in managing complex projects in...

Job Title: Clinical Documentation Specialist - US HealthcareSalary Range: 8-9 LPA (Indian Rupees per Annum)About the RoleWe are seeking a highly skilled Clinical Documentation Specialist to join our team at Heart Vascular and Leg Center. This is a unique opportunity to work with our healthcare providers in the US, documenting clinical encounters and managing...

The Company OverviewNulife, an ISO-13485 certified medical disposables company, has been serving humanity for 59 years. Headquartered in Mumbai, we have 4 locations across India with a network of more than 3000 channel partners. Our products are sold globally in over 80 countries and enjoy a global reputation for products that offer superior protection, high...

Talentgigs is seeking an experienced Senior Clinical Full Stack Software Engineer to join our team. With a focus on developing clinical applications, this role requires a strong understanding of healthcare workflows and regulations.Salary: The estimated annual salary for this position is around $120,000 - $180,000 depending on experience and...

Excelya is a leading Contract Research Organization (CRO) in Europe, founded in 2014 with its headquarters in Paris. With over 900 experts globally, the company provides trial solutions across various therapeutic areas. Excelya's one-team approach to work ensures that collaboration is at every stage of a project, from regulatory affairs and clinical...

Seeking a skilled Clinical Data Manager II to oversee data collection, management, and reporting for clinical trials. As a member of our team, you will ensure data accuracy, security, and compliance with regulatory standards.About the RoleThis position involves managing multiple concurrent studies, leading a team of data coordinators, and collaborating with...

Company OverviewAdvanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience, and innovation.We help our...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to lead our Regulatory Publishing team. The ideal candidate will have 6+ years of experience in eCTD Regulatory Publishing and strong knowledge of eCTD process.Key Responsibilities:Liaise with cross-functional teams to ensure compliance with government acts and regulations.Oversee...

Excelya, a leading Contract Research Organization (CRO) in Europe, is seeking a part-time Quality Control Specialist to join their team. Based in India and working remotely, this role requires excellent English language skills.About ExcelyaAs one of the top CROs in Europe, Excelya was founded in 2014 and is headquartered in Paris. With over 900 experts...

Job DescriptionA Medical Document Quality Assurance Specialist at ARDEM Data Services plays a pivotal role in ensuring the accuracy, quality, and compliance of medical documents. This position is ideal for individuals with a strong attention to detail and excellent communication skills.ResponsibilitiesDocument Review: Conduct thorough reviews of various...

Job OverviewWe are seeking a highly skilled Medical Data Analyst to join our team at ARDEM Data Services. This role is essential in ensuring the accuracy, quality, and compliance of medical documents with regulatory standards.About the RoleDocument Review: Conduct thorough reviews of various medical documents, including clinical trial reports, regulatory...

We are seeking a highly skilled Clinical Data Solutions Expert to join our team at Talentgigs. The ideal candidate will have 4-6 years of experience in SQL development with a strong background in the clinical domain.Job SummaryThe Clinical Data Solutions Expert will be responsible for designing, developing, and maintaining complex SQL queries, stored...

Transforming Clinical DataA highly skilled Clinical Data Management Lead is sought by Lifelancer to lead multiple clinical trials from protocol review to database lock. With 10 years of experience in the pharmaceutical industry or CRO environment, you will ensure data is collected, managed, and reported accurately and securely.About the RoleLead data...