Clinical Contracts Specialist II, Site Agreements

Job SummaryMUM Fortrea Development India Pvt Ltd is seeking a highly skilled Clinical Contract Specialist II to join our team. As a key member of our clinical operations team, you will be responsible for negotiating and managing site agreements and contracts for clinical studies.Key ResponsibilitiesAdhere to standard operating procedures (SOPs) and ensure...

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 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,...

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)...

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 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...

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...

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...

Key Responsibilities:Site Management: Primary contact with investigative sites during study maintenance and start-up activities, ensuring timely collection of required documents for EC/IRB/Third body/Regulatory Authority submissions.Regulatory Awareness: Develop and maintain awareness of regulatory legislation, guidance, and practice in assigned countries...

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...

Partner One Capital is a leading enterprise software group, and we are seeking a highly skilled Software Licensing Agreement Specialist to join our team. As a Specialist, you will be responsible for reviewing, redlining, and negotiating complex software licensing agreements with our clients.Key responsibilities include:Drafting and reviewing software...

Job SummaryThe Clinical Collaboration Specialist will play a key role in initiating and managing clinical and research collaborations at hospitals, medical centers, and academic institutions globally and regionally. This position will work closely with internal and external stakeholders, including Clinical and Regulatory Affairs, Innovations, Product...

Overview:At Lifelancer, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change.A market leader and pioneer, Lifelancer breaks the silos...

Job SummaryPSI is seeking a highly skilled Clinical Trial Startup Specialist to join our team in Bangalore. As a key member of our project team, you will be responsible for ensuring the smooth and timely startup of clinical projects in India.Key ResponsibilitiesDevelop site-specific startup timelines and meet site activation targetsProvide progress updates...

Job Summary:The Clinical Operations Assistant will be responsible for maintaining the Central Files for Clinical Operations, ensuring efficiency, accuracy, and quality. This role will involve tracking, scanning, filing, and entry of Case Report Forms to clients for assigned projects. The COA will also support site management team members on local billable...

George Clinical is a leading global clinical research organization driven by scientific expertise and operational excellence. With over 20 years of experience, our team manages 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe, offering full-range clinical trial services to biopharmaceutical, medical device, and diagnostic...

Job SummaryWe are seeking a skilled Clinical Trials Contract Specialist 2 to join our global team at Lifelancer. In this role, you will be responsible for ensuring the timely and efficient management of clinical trials contracts, ensuring compliance with regulatory requirements and company policies.Key Responsibilities:Manage clinical trials contracts from...

As a leading global contract research organization (CRO), 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.Key Responsibilities:Support the payment of assigned studies, including study set-up, maintenance,...

Clinical Operations AssistantThe role of the Clinical Operations Assistant is to ensure the accuracy and quality of the Central Files for Clinical Operations. The position will be based in India, working with teams in Japan, and supporting the delivery of work in country. Key responsibilities include tracking, scanning, filing, and entry of Case Report Forms...

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,...