Clinical Contract Specialist II

Key Responsibilities:As a Clinical Contract Specialist II at MUM Fortrea Development India Pvt Ltd, you will be responsible for ensuring adherence to standard operating procedures (SOPs) and performing daily tracking, negotiation, and approval of Site Agreements and Site Agreement templates for clinical study teams. You will also be responsible for timely...

Job SummaryFortrea Development India Pvt Ltd is seeking a highly motivated and detail-oriented Clinical Contract Specialist II to join our team. As a key member of our clinical operations team, you will be responsible for managing site agreements and ensuring compliance with internal processes and procedures.Key ResponsibilitiesManage site agreements and...

Job SummaryAs a leading global contract research organization (CRO), Fortrea is seeking a highly motivated and detail-oriented Clinical Contracts Specialist II to join our team. The successful candidate will be responsible for managing site agreements and ensuring compliance with internal processes and procedures.Key ResponsibilitiesResponsible for adherence...

Role Summary:George Clinical is seeking a highly skilled Clinical Research Specialist to join our team. As a Clinical Research Specialist, you will provide medical and academic input to various aspects of George Clinical studies.Key Responsibilities:Provide medical and academic expertise for new and existing George Clinical studies.Support Endpoint...

Job SummaryWe are seeking a highly motivated and detail-oriented Site Contracts Specialist to join our team at BAN Fortrea Clinical Development Pvt Ltd. The successful candidate will be responsible for managing site contracts and ensuring compliance with regulatory requirements.Key ResponsibilitiesDevelop and maintain awareness of regulatory legislation,...

Job SummaryWe are seeking a highly motivated Site Contracts Specialist to join our team at BAN Fortrea Clinical Development Pvt Ltd. The successful candidate will be responsible for coordinating with investigative sites during study maintenance and start-up activities, ensuring timely collection of essential documents for submission to regulatory...

Key Responsibilities:As a key member of our Site Agreements team, you will be responsible for ensuring adherence to standard operating procedures (SOPs) and performing daily tracking, negotiation, and approval of Site Agreements and Site Agreement templates. You will also be responsible for updating the departmental Site Agreement Management System (SAMS)...

Clinical Data Analyst IIAbout the Role:The Clinical Data Analyst II is a key member of the Clinical Study Team, responsible for performing clinical data validation activities on assigned projects. This role requires strong technical aptitude, attention to detail, and excellent problem-solving skills.Key Responsibilities:Perform data validation activities,...

We are expanding our global clinical research capabilities and are seeking a highly skilled medical professional to join our team as a Medical Monitor. As a Medical Monitor, you will be responsible for providing medical and academic input to various aspects of our clinical studies, ensuring project delivery is of high quality, operationally aligned,...

Job Title: Clinical Trial Startup SpecialistAt PSI, we are seeking a skilled Clinical Trial Startup Specialist to provide operational support to project teams in India. The ideal candidate will ensure that PSI clinical projects start smoothly and on time.Key Responsibilities:Develop site-specific startup timelines and meet site activation targetsProvide...

Job SummaryFortrea Development India Pvt Ltd is seeking a highly skilled Clinical Data Specialist to join our team. As a Clinical Data Specialist, you will be responsible for reviewing clinical trial data in accordance with global data management plans and applicable standardized data management processes. You will identify erroneous, missing, incomplete, or...

Key ResponsibilitiesAs a Clinical Development Specialist at MUM Fortrea Development India Pvt Ltd, you will be responsible for adhering to standard operating procedures (SOPs) and performing various tasks with minimal guidance. Key tasks include:Tracking, negotiating, and approving Site Agreements and Site Agreement templates for clinical study...

As a leading global contract research organization, Fortrea provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.Our team is seeking a highly skilled Clinical Data Specialist to perform the clinical medical data coding...

Job DescriptionJob Title: Clinical Data SpecialistMUM Fortrea Development India Pvt Ltd is seeking a highly skilled Clinical Data Specialist to join our team.Responsibilities:Review clinical trial data in accordance with global data management plans and applicable standardized data management processes.Run ancillary programs to support data review...

Lifelancer, a talent-hiring platform in Life Sciences and IT, offers an exciting opportunity for a Global Contracting Specialist. This role involves working with clients to develop proper internal controls using analytics and technology solutions.Job Description:We are seeking a dynamic individual to join our Global Contract Practice. The ideal candidate...

Job Title: Medical Data Review Specialist IIFortrea Development India Pvt Ltd is seeking a highly skilled Medical Data Review Specialist II to join our team. As a key member of our Global Medical Data Review Team, you will be responsible for executing Central Medical Review activities and assisting senior staff and Medical Monitors in their...

The OpportunityWe are seeking a highly skilled Clinical Research Scientist II to join our team at Teva Pharmaceuticals. As a key member of our research team, you will be responsible for screening activities, including obtaining informed consent from volunteers, performing general physical and medical examinations, and reviewing various reports.Key...

Job SummaryFortrea is seeking a highly skilled Clinical Data Specialist to join our team. As a Clinical Data Specialist, you will be responsible for performing clinical medical data coding aspects of assigned projects with supervision.Key ResponsibilitiesWork with the technical service group staff and aide in personal career development, interpersonal...

Job SummaryWe are seeking a highly skilled and detail-oriented Clinical Data Analyst II to join our team at Parexel. As a Clinical Data Analyst II, you will be responsible for performing clinical data validation activities on assigned projects, ensuring compliance with corporate quality standards, SOPs, ICH-GCP, and international regulatory requirements.Data...

Job Summary: We are seeking a skilled Medical Data Review Specialist II to join our Global Medical Data Review Team. The successful candidate will be responsible for the execution of key Central Medical Review activities and will assist senior staff and Medical Monitors in the execution of their responsibilities.Key Responsibilities:Collaborate with the...