8306 Clinical Research Jobs - Page 4

Role Description: The Study Delivery Associate provides essential administrative and operational support to clinical trial management activities. This role supports the Study Delivery T eam in meeting study timelines, ensuring regulatory compliance, and executing standardized processes related to clinical trial coordination, document and system management. The Study Delivery Associate may also support specialized activities to promote expertise , quality, and consistency across studies. Key responsibilities include maintaining accurate and timely data within clinical systems (e.g., CTMS) and supporting study training and related operational requirements. Roles & Responsibilities: Study Coord...

Role Overview: As a Feasibility Lead in Business Development, you will be responsible for driving country and site feasibility activities for early-phase clinical trials. Your role will involve analyzing feasibility data, collaborating with internal teams and external clients, and providing strategic recommendations to support study planning and proposal development. Your critical role will focus on aligning feasibility operations with scientific, operational, and regulatory goals across global regions. Key Responsibilities: - Act as the go-to expert for feasibility practices across therapeutic areas. - Provide strategic input on site and country selection during protocol development. - Stay...

Project Title: Development of phyto-formulation to combat acaricidal resistance tick infestation in field conditions using an integrative approach. Name of Post - Project Research Scientist-I (Non Medical) No. posts - 01 Essential Qualification Experience - Post Graduate Degree, including the integrated PG degrees Desirable Qualification Experience - Candidate with experience in parasitology / vector biology / molecular biology / phytochemical evaluation. Experience in handling tick samples, tick bioassay work and phyto-formulation with large animal trials will be preferred. Consolidated Emolument- Rs.56000/- +HRA, as admissible Duration:- Initially for 1 year (extendable as per project dura...

Job Posting Title India Bengaluru - hybrid Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients lives and act accordingly. We strive t...

Process Improvement Initiatives Develop and lead focused process improvement initiatives to ensure positive system hospital adoption of processes and products, demonstrating improved patient outcomes Educate the physicians, anesthesiologists, intensivists, and nursing staff in both OR and ICU settings on the clinical value of the technologies Provide in-theatre support and guidance during surgical procedures and bedside support in ICUs involving advanced hemodynamic monitoring for clinical decision-making Research data, partner with data experts, set strategy for key metrics, and present baseline and outcome findings to key stakeholders Ensure optimal technology adoption and improved patient...

Nandadeep Eye Hospital is looking for Pharmacist-Sangli to join our team Roles and Responsibility Dispense medications to patients and provide counseling on their proper use. Manage inventory and maintain accurate records of prescriptions and stock levels. Collaborate with healthcare professionals to develop and implement medication therapy plans. Conduct regular patient assessments to identify potential medication interactions or side effects. Develop and implement policies and procedures for medication management. Provide training and support to staff members on medication-related topics. Job Requirements Bachelor's degree in Pharmacy (B.Pharm) from a recognized institution. Minimum years ...

Novartis India is looking for Senior Scientific Writer to join our team Roles and Responsibility Develop high-quality scientific content for various publications. Collaborate with cross-functional teams to create engaging and informative content. Conduct research and analyze data to stay updated on industry trends. Create and edit manuscripts, reports, and other scientific documents. Ensure accuracy, clarity, and consistency in all written materials. Meet deadlines and deliver high-quality results. Job Requirements Strong understanding of scientific principles and practices. Excellent writing, editing, and communication skills. Ability to work independently and as part of a team. Strong anal...

ThinkRoman is looking for Senior Medical Representative Warangal, Adilabad, TamilNadu,Bihar(Patna) to join our team Roles and Responsibility Develop and implement effective sales strategies to achieve business objectives. Build and maintain strong relationships with key customers and stakeholders. Conduct market research and analyze industry trends to identify new opportunities. Collaborate with cross-functional teams to launch new products and services. Provide excellent customer service and support to clients. Achieve sales targets and contribute to company growth. Job Requirements Strong knowledge of medical representative activities and pharmaceutical sales. Excellent communication and i...

Dalvkot Utility Enterprises Private Limited is looking for Pharmacist to join our team Roles and Responsibility Dispense medications to patients and provide counseling on their proper use. Manage inventory and maintain accurate records of prescriptions and stock levels. Collaborate with healthcare professionals to develop and implement medication therapy plans. Conduct regular patient assessments to identify potential medication interactions or side effects. Develop and implement pharmacy protocols and procedures. Participate in quality improvement initiatives to enhance patient care and safety. Job Requirements Bachelor's degree in Pharmacy (B.Pharm) or equivalent qualification. Minimum yea...

Intas Pharmaceuticals is looking for Research Associate UPD to join our team Roles and Responsibility Conduct experiments and collect data to support research projects. Analyze and interpret complex data sets to draw meaningful conclusions. Develop and implement new research methods and techniques. Collaborate with cross-functional teams to achieve project goals. Prepare and present research reports and findings to stakeholders. Stay updated with industry trends and developments. Job Requirements Strong understanding of research principles and methodologies. Excellent analytical and problem-solving skills. Ability to work independently and as part of a team. Effective communication and inter...

ICON plc is looking for Site Specialist II to join our team Roles and Responsibility Manage and coordinate site operations for efficient project execution. Conduct regular site inspections to monitor progress and identify potential issues. Collaborate with cross-functional teams to resolve site-related problems. Develop and implement effective site management plans to meet project goals. Analyze data and reports to optimize site performance and improve outcomes. Ensure compliance with company policies and procedures. Job Requirements Strong understanding of site operations and management principles. Excellent communication and problem-solving skills. Ability to work effectively in a fast-pac...

Cyber Security Academy Southampton is looking for Clinical Research Fellow in Infectious Diseases to join our team Roles and Responsibility Conduct clinical research studies on infectious diseases, including data collection, analysis, and interpretation. Collaborate with cross-functional teams to develop and implement research protocols and procedures. Develop and maintain databases and spreadsheets to track study progress and results. Prepare and present research reports and findings to stakeholders. Participate in quality control and quality assurance activities to ensure compliance with regulatory requirements. Stay up-to-date with industry developments and advancements in infectious dise...

Acko is looking for Clinical Ops Intern to join our team Roles and Responsibility Assist in the development and implementation of clinical operations processes. Collaborate with cross-functional teams to ensure seamless execution of clinical trials. Develop and maintain accurate records of clinical trial data. Support the preparation of regulatory documents and reports. Ensure compliance with regulatory requirements and company policies. Participate in quality improvement initiatives to enhance clinical operations efficiency. Job Requirements Strong understanding of clinical operations principles and practices. Excellent communication and interpersonal skills. Ability to work effectively in ...

Department MedComm, Rare Disease Product and Portfolio strategy (P&PS) Location Bangalore, Novo Nordisk Global Business Services (GBS), India Are you an experienced medical communication professional with a passion for delivering high-quality, compliant scientific contentDo you thrive in a collaborative and strategic environmentIf so, we invite you to join Novo Nordisk as our new Global Scientific Advisor and make a difference in the Rare Disease therapy area portfolio Read on and apply today! About The Department MedComm, Rare Disease Product and Portfolio Strategy (P&PS), headquartered in Zurich (HQ), is part of Global Business Services (GBS), Bangalore, India The team is composed of highl...

For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality compliance, pharmacovigilance, medical information, and RD technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device...

The candidate must possess in-depth functional knowledge of the process area and apply it to operational scenarios to provide effective solutions. The candidate must be able to identify discrepancies and propose optimal solutions by using a logical, systematic, and sequential methodology. It is vital to be open-minded towards inputs and views from team members and to effectively lead, control, and motivate groups towards company objects. Additionally, the candidate must be self-directed, proactive, and seize every opportunity to meet internal and external customer needs and achieve customer satisfaction by effectively auditing processes, implementing best practices and process improvements, ...

Role & responsibilities Ensures clinical trials are conducted at assigned sites as per protocol, local regulatory requirements, ICH GCP, ensure data integrity, patient safety and trials are conducted as per ethical standards (declaration of Helsinki). Act as primary communication point between SPIL and clinical trial site w.r.t site management activities. Facilitating regulatory submission Train and Mentor CRAs as applicable Support RTL’s on trial management tasks as delegated Perform Accompanied site visits with CRA’s where required and applicable. Take part in Quality Oversight activities as assigned by RTL’s Perform site feasibilities, ensure site database is updated on periodic basis wit...

Role & responsibilities Ensures clinical trials are conducted at assigned sites as per protocol, local regulatory requirements, ICH GCP, ensure data integrity, patient safety and trials are conducted as per ethical standards (declaration of Helsinki). Act as primary communication point between SPIL and clinical trial site w.r.t site management activities. Facilitating regulatory submission Train and Mentor CRAs as applicable Support RTLs on trial management tasks as delegated Perform Accompanied site visits with CRAs where required and applicable. Take part in Quality Oversight activities as assigned by RTL’s Perform site feasibilities, ensure site database is updated on periodic basis with ...

Role GCF: 3 ABOUT THE ROLE Role Description: The Study Delivery Associate provides essential administrative and operational support to clinical trial management activities. This role supports the Study Delivery T eam in meeting study timelines, ensuring regulatory compliance, and executing standardized processes related to clinical trial coordination, document and system management. The Study Delivery Associate may also support specialized activities to promote expertise , quality, and consistency across studies. Key responsibilities include maintaining accurate and timely data within clinical systems (e.g., CTMS) and supporting study training and related operational requirements. Roles & Re...

Role Name: Study Delivery Associate Role GCF: 3 Role Description: The Study Delivery Associate provides essential administrative and operational support to clinical trial management activities. This role supports the Study Delivery Team in meeting study timelines, ensuring regulatory compliance, and executing standardized processes related to clinical trial coordination, document and system management. The Associate may also contribute to SSU Hub activities to promote expertise, quality, and consistency across studies. Key responsibilities include maintaining accurate and timely data within clinical systems (e.g., CTMS) and supporting study training and related operational requirements. Role...

Works directly with the Head of Pharmacovigilance and Medical Monitoring, in managing both corporate and project-related activities Cooperates directly with Safety Monitors, Project Leadership, Data Managers and other relevant functional groups At the project level, will function in the role of a Medical Monitor leading the clinical trial monitoring of safety and efficacy data for the assigned protocols in scope of the contract with the client and in compliance with relevant SOP and/or other relevant study specific documents Provides safety oversight throughout the lifecycle of the clinical study including evaluation, assessment, and monitoring of safety events and protocol deviations Cooper...

Primary Responsibilities: To provide medical expertise in related TA and its product portfolio, including affiliate, regional and global teams, contributing to medical strategies and brand commercialization. Ensure detailed, current knowledge of the respective Molecule(s) data. And contribute to scientific and medical expertise to develop effective partnerships with relevant functions, including Pricing Reimbursement & Access (PRA), Clinical Operations, Corporate Affairs, Human Resources, Legal, Marketing, Medical Information, Global Product Safety and Training. To develop effective partnerships with clinicians, other key influencers and external groups. To provide visible leadership to othe...

Role Description: The Study Delivery Senior Associate provides essential global operational support to clinical study teams, ensuring timely , high-quality, and compliant study execution. They complete assigned by the Study Managers and Leads start-up and conduct activities, own specific study tasks, support with monitor ing for risks or issues, and escalate early warning signals with proposed solutions to relevant stakeholders. Roles & Responsibilities: Study Planning & Coordination Support and sometimes own the development and maintenance of study-level trackers, dashboards, timelines, and tools (e.g., vendor management, sample tracking, drug supply planning) to ensure accuracy and visibil...

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