8317 Clinical Research Jobs - Page 9

Job Type: Part-Time / Hourly -Remotely from anywhere across India / Globally. Job Position : Medical Director / Sr.Consultant -Medical Oncology. Job Location: Noida / Gurgaon / anywhere in India OR Global Job Description: We are currently looking for Medical Oncologist with strong experienced in Medical Oncology with an entrepreneur mindset prepared to work in a collaborative Team as our Internal Team member / Partner/ External Partner / having busy Medical Oncology Practices handled atleast 100-10000's of Cancer Patients ( In top 20 Cancers) in his experience with a reputed Medical Research University & Hospital or in a startup /mid-size company/ MNC / Top Onco Pharma MNC. Qualification : 1...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Roles and Responsibility Manage and coordinate clinical trial activities, including protocol development, site initiation, and data management. Develop and implement effective clinical trial strategies to ensure successful study execution. Collaborate with cross-functional teams, including medical writing, biostatistics, and regulatory affairs. Conduct site feasibility assessments and provide guidance on study design and methodology. Ensure compliance with regulatory requirements and company policies. Provide training and support to internal staff and external partners. Job Requirements Bachelor's degree in life sciences or a related field. Minimum 5 years of experience in clinical trials ma...

Roles and Responsibility Develop and implement effective drug safety strategies to ensure compliance with regulatory requirements. Conduct thorough reviews of clinical trial data to identify potential safety concerns. Collaborate with cross-functional teams to resolve safety-related issues and improve overall patient safety. Stay up-to-date with changing regulations and industry trends in drug safety. Provide expert guidance on drug safety matters to internal stakeholders. Analyze complex data sets to identify trends and patterns in drug safety. Job Requirements Strong knowledge of drug safety regulations and guidelines. Excellent analytical and problem-solving skills. Ability to work effect...

Roles and Responsibility Conduct thorough reviews of clinical trial data to identify potential safety concerns. Develop and implement effective pharmacovigilance strategies to mitigate risks. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze complex data sets to identify trends and patterns that may impact patient safety. Prepare detailed reports and presentations to communicate findings to stakeholders. Stay up-to-date with changing regulations and industry standards in pharmacovigilance. Job Requirements Strong knowledge of pharmacovigilance principles and practices. Excellent analytical and problem-solving skills. Ability to work effectivel...

Roles and Responsibility Conduct thorough medical examinations and diagnose patients' conditions. Develop and implement effective treatment plans. Collaborate with other healthcare professionals to provide comprehensive care. Stay updated with the latest medical research and advancements. Provide guidance and support to junior staff members. Participate in quality improvement initiatives to enhance patient outcomes. Job Requirements Strong knowledge of medical principles and practices. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environment. Strong analytical and problem-solving skills. Commitment to delivering high-quality patient care. Abil...

Roles and Responsibility Operate and maintain various imaging equipment, including X-ray machines and CT scanners. Prepare patients for procedures, explain the process, and ensure their safety during imaging. Interpret images taken by other medical professionals, such as radiologists and nurses. Maintain accurate records of patient information and imaging results. Collaborate with healthcare teams to provide high-quality patient care. Stay updated on new technologies and techniques in imaging. Job Requirements Bachelor's degree in Medical Technology or a related field. At least 2 years of experience in an imaging department, preferably in a hospital or clinic setting. Strong knowledge of med...

Roles and Responsibility Operate and maintain various imaging equipment, including X-ray machines and CT scanners. Prepare patients for procedures, explain the process, and ensure their safety during imaging. Interpret images taken by other medical professionals, such as radiologists and nurses. Maintain accurate records of patient information and imaging results. Collaborate with healthcare teams to provide high-quality patient care. Stay updated on new technologies and techniques in imaging. Job Requirements Bachelor's degree in Medical Technology or a related field. At least 2 years of experience in an imaging department, preferably in a hospital or clinic setting. Strong knowledge of med...

Roles and Responsibility Provide expert medical advice and guidance to clients on various health-related matters. Conduct thorough medical research and analysis to stay updated with the latest developments in the field of medicine. Collaborate with cross-functional teams to develop and implement effective treatment plans. Develop and maintain relationships with key stakeholders, including healthcare professionals and industry partners. Stay current with regulatory changes and updates in the medical field. Participate in quality improvement initiatives to enhance patient outcomes. Job Requirements Strong knowledge of medical practices and regulations. Excellent communication and interpersonal...

Roles and Responsibility Manage and oversee clinical projects from initiation to completion, ensuring timely and within-budget delivery. Develop and implement project plans, resource allocation, and risk management strategies. Collaborate with cross-functional teams, including medical, scientific, and operational staff. Conduct project meetings, progress updates, and status reports to stakeholders. Identify and mitigate potential risks, issues, and dependencies impacting project timelines or budgets. Ensure compliance with regulatory requirements, company policies, and industry standards. Job Requirements Strong understanding of clinical trial operations, including protocol development, site...

Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer Manage day-to-day workload: identify project needs, track timelines and implement customer requests, keeping manager/senior staff abreast of progress on tasks and any potential problems with project work Lead customer meetings independently give presentation to an existing customer (eg to discuss templates, results, lessons learned), responding appropriately to feedback deliver basic level training to small groups or individuals...

We are seeking a seasoned BMC Discovery Subject Matter Expert (SME) to lead enterprise-wide discovery initiatives This role will focus on designing, implementing, and optimizing BMC Discovery solutions to ensure accurate visibility of IT assets and dependencies In addition, the SME will coordinate with Mergers & Acquisitions (M&A) teams and project stakeholders to deploy and integrate other software discovery agents, ensuring seamless visibility and compliance across diverse environments The ideal candi will combine deep technical expertise with strong collaboration skills to support IT operations, CMDB accuracy, and business transformation initiatives Roles and responsibilities: Lead the de...

Good Communication skills, Attention to Details, Pharma Knowledge, Marketing ideas Assist in writing, coordination and management of RCT PMS, RWE based studies Ensure compliance with regulatory guidelines and ethical standards and ethical dossier preparation Participate in pre-study site visit, study meetings and field work Review and assist in the creation of informed consent forms and recruitment materials Schedule and coordinate patient visits for trials Assist with data entry and ensure accurate recording of patient data and study outcomes in confidentiality Prepare and participate in progress meetings with the research team Assist in maintaining the study inventory, including investigat...

Programmatic Activation Specialist IQVIA is the leading global provider of data, advanced analytics, technology solutions and clinical research services for the life sciences industry IQVIA Digital powers exceptional brand experiences, delivering innovative solutions based on a customer-first, insights-driven, and integrated omnichannel vision We provide authenticated, enhanced data and analytics, innovative fit-for-purpose healthcare technology, and the expertise to enable an effective and adaptable marketing model that drives better quality of care and patient outcomes Role: Programmatic Traders are executional experts responsible for the setup, optimization, and performance management of ...

In this role, you ll be managing multiple large and complex global consulting projects for clients in the life science industry. This exciting opportunity will allow you to lead project teams to provide solutions to clients and identify further areas to support our clients to drive healthcare forward. What You ll Be Doing Planning, organizing, and managing a team for successful project completion Managing stakeholders in large (multi-workstream) projects, including seniors, cross-functional teams and clients Designing, structuring, and delivering client reports and presentations Developing client relationships and identifying opportunities for follow-on work and new leads Supporting the deve...

Assists in performing safety monitoring activities in cooperation with project Medical Monitor/Medical Officer and other relevant project team members Reviews safety events Assists in the collection, assessment, monitoring, review and reporting of adverse drug reaction cases from all sources - clinical (both interventional and non-interventional), data sets analyzed in association with RWE projects, spontaneous reports, literature, etc Provides first line evaluation of serious adverse events (SAEs) communicate with site staff regarding reported AEs or SAEs to gather additional information Subject to review by a senior team member, prepares a summary narrative for each reported SAE suitable f...

Acts as an SME on eTMF applications, TMF processes, document identification/filing and project team processes that result in TMF document generation/collection Owns the TMF Plan/Index and leads the identification of expected documents by finding ways and means to stay abreast of the study events Review the SoW to understand the scope of work and align TMF requirement to it Delineate between in scope vs out of scope TMF activities Build relationships with sponsor counterpart keeping Project Manager/Leader in loop to partner with them and provide inputs on best industry practices, especially if sponsor eTMF is used for assigned studies Ensures the TMF file structure follows applicable company ...

Required Qualifications: Bachelor s degree in computer science or a related field, with at least 8 years of experience in the pharmaceutical industry. A minimum of 6 years of experience in clinical trial database design and management, specifically with EDC systems such as Medidata Rave, including experience with Rave EDC Custom Function programming. Experience with clinical research and database development within the pharmaceutical industry, as we'll as Agile methodologies. Proficiency with database structures and programming languages. Expertise in eCRF design and specifications development. Experience writing, programming, or configuring data validation checks. Familiarity with QC, UAT, ...

Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Construction of single and double gene expression vectors. Transfection of CHO-GS (-) cell lines for generating and finalization of minipools. Understanding in development of GMP cell banks for process development. Responsible for delivering robust clones for p...

Construction of single and double gene expression vectors. Transfection of CHO-GS (-) cell lines for generating and finalization of minipools. Understanding in development of GMP cell banks for process development. Responsible for delivering robust clones for process development. Work closely with process teams in transferring clones for process development. Single cell seeding of the minipools for monoclone generation. Planning and executing fed batch studies of minipools as we'll as monoclones for titre as we'll as quality analysis. Preparation of department specific SLPs and SOPs. Preparation and review of cell line development reports for mammalian as we'll as microbial projects. Managem...

Operate hematology, biochemistry, coagulation ad urine analyzers and perform testing of QC/ patients/subjects/EQAS samples as per procedure defined in the SOPs. EQAS samples results analysis and evaluation in timely manner. To update section in-charge for requires stock/inventory on monthly or as and when required. Instrument Maintenance and troubleshooting in routine operations as and when required. To preformed samples accession related activities, temp. recording & instrument date backup. Any other responsibilities assigned by management / HOD. EDUCATIONAL QUALIFICATION B.Sc./M.Sc., MLT

Job Summary: Assistant Manager Clinical Trials will lead and manage clinical trials and research studies, ensuring that they are completed on time, within budget, and in compliance with regulatory standards. The assistant manager will supervise research teams, collaborate with cross-functional departments, and provide strategic direction for clinical research activities. Key Responsibilities: 1. Clinical Trial Management: Plan, initiate, and manage clinical research projects from start to finish. Coordinate and oversee the execution of clinical trials, ensuring adherence to protocols, timelines, and budgets. Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and et...

We are seeking a seasoned BMC Discovery Subject Matter Expert (SME) to lead enterprise-wide discovery initiatives. This role will focus on designing, implementing, and optimizing BMC Discovery solutions to ensure accurate visibility of IT assets and dependencies. In addition, the SME will coordinate with Mergers & Acquisitions (M&A) teams and project stakeholders to deploy and integrate other software discovery agents, ensuring seamless visibility and compliance across diverse environments. The ideal candidate will combine deep technical expertise with strong collaboration skills to support IT operations, CMDB accuracy, and business transformation initiatives. Roles and responsibilities: Lea...

Acts as Lead Medical Writer on more advanced writing projects (e. g. complex clinical study reports, protocols, more challenging indications, or customers). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. May provide feedback to peers when asked for input or review. Negotiates timelines and discusses/resolves customer comments. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing. Essential Functions Take a leading role in preparing as...

Senior Manager, Central Support Services - Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Manager, Central Support Services to join our diverse and dynamic team. As a Senior Manager, Central Support Services at ICON, you will be crucial in overseeing and optimizing our central support functions to enhance organizational efficiency and effectiveness. You will lead a team dedicated to providing essential support services across various dep...