3711 Clinical Research Jobs - Page 41

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...

- Collaborate with project managers to define scope, timelines, and deliverables - Ensure timely and effective execution of clinical trial software solution projects - Provide consulting for CTMS platform implementation, configuration Required Candidate profile - Advise on solution architecture, workflows, and usability enhancements in CTM systems - Validate the alignment of software features with clinical workflows and regulatory requirements Perks and benefits -GPA &term Insurance -5 days week -open to discuss

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT && HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Qualification & Specifications : MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry). Skills Required: * Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). Role: To review US medical records Initial file review for identifying merits Subjective review and analysis to identify instances of...

Project Role: Centralized Monitoring Lead Work Experience: 4 plus years of CRA and Clinical trials and monitoring. Work location: Bangalore/Thane/Pune/Ahmedabad/Kochi/Hyderabad Work Mode: Hybrid/Office Based Shift: 2.00pm to 11.00pm Must Have Skills: Onsite / Remote / Risk Based Monitoring, Clinical Research, Clinical trials. Job Responsibility: Oversight of clinical deliverables across all trial phases (start-up to close-out). Development and review of study management plans, risk assessments, and analytics strategies. • Monitoring of site performance, key risk indicators (KRIs), and operational triggers. Financial oversight including budget tracking and investigator payments. Coordination ...

Key Responsibilities: Manage the entire slot game production lifecycle from concept to launch and post-launch support Coordinate with designers, developers, artists, animators, sound designers, and QA teams Develop and maintain project schedules, budgets, and resource plans Communicate project status, risks, and milestones to stakeholders and senior management Ensure all slot games comply with industry standards and regulatory requirements Drive team collaboration and maintain a productive work environment Identify and implement process improvements to enhance efficiency and quality Support marketing and business development teams with launch strategies and promotional activities

Purpose The role of the Principal Statistician is to provide statistical support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Principal Statistician may also perform a supervisory role (e.g. line management and/or project management). Key Responsibilities Development of Methods Table: The candidate will lead the effort to develop and refine versions of the methods table, which will list methodologies required for clinical trial reporting and align those methods to existing R packages or identify gaps to be filled. Collaboration with various SMEs and regular reviews with experts will be essential. Package Review: - The candidate s...

Key Responsibilities: Manage the entire slot game production lifecycle from concept to launch and post-launch support Coordinate with designers, developers, artists, animators, sound designers, and QA teams Develop and maintain project schedules, budgets, and resource plans Communicate project status, risks, and milestones to stakeholders and senior management Ensure all slot games comply with industry standards and regulatory requirements Drive team collaboration and maintain a productive work environment Identify and implement process improvements to enhance efficiency and quality Support marketing and business development teams with launch strategies and promotional activities

Purpose The role of the Principal Programmer is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. Key Responsibilities The study programmer position will be responsible for manipulating large databases and generating reports to enable analysts to explore real world healthcare data assets. Candidates must have excellent SAS and SQL programming skills and the ability to implement complex logic. Candidates must be comfortable with creating complex analysis data sets derived from various data sources with a careful eye for outliers and errors. Prior experience building patient cohorts and evaluating patient heal...

Roles and Responsibilities Work at a medical store as a pharmacist. Desired Candidate Profile Must have a Maharashtra pharmacist license Perks and Benefits Accommodation is available in Prabhadevi near the store.

As the Medical Science Liaison, your primary responsibility is to develop and maintain in-depth knowledge of assigned products and relevant therapeutic areas. This involves actively participating in internal meetings, training sessions, congresses, seminars, and staying updated with national and international literature through self-study. You will be expected to provide expert medical and scientific advice for assigned products, respond to requests for scientific information, and contribute to the development of core dossiers. Building and nurturing professional relationships with key opinion leaders and academic centers will be crucial, including organizing and participating in scientific ...

About the job: Key responsibilities: 1. Perform routine laboratory tests and procedures as per medical protocols. 2. Prepare, collect, and process biological samples (blood, tissue, etc.). 3. Maintain accurate records of lab reports and ensure timely delivery to doctors. 4. Calibrate, operate, and maintain lab equipment and instruments. 5. Ensure compliance with safety and hygiene standards within the lab. 6. Support doctors and medical staff during diagnostic procedures and OT (where required). 7. Manage inventory of lab supplies and request replenishment when needed. 8. Adhere to QHT Clinic's quality standards and maintain confidentiality of patient data. Who can apply: Only those candidat...

Job Title: Medical Oncologist Location: [Silchar,Assam,India] Department: Oncology Job Type: [Full-Time] Position Summary: We are seeking a dedicated and compassionate Medical Oncologist to join our multidisciplinary oncology team. The successful candidate will be responsible for diagnosing and treating patients with cancer using chemotherapy, hormonal therapy, biological therapy, and targeted therapy. The role requires collaboration with surgical oncologists, radiation oncologists, pathologists, radiologists, and palliative care specialists to deliver comprehensive cancer care. Key Responsibilities: Evaluate, diagnose, and manage patients with various types of cancer. Develop and implement ...

We are looking for a highly skilled Mechanical HVAC Design professional with 7 to 9 years of experience to join our team at AECOM India Private Limited, located in the Cement/Construction/Engineering/Metals/Steel/Iron industry. Roles and Responsibility Design and develop mechanical systems for HVAC applications. Collaborate with cross-functional teams to ensure successful project execution. Conduct site visits to monitor progress and resolve technical issues. Develop and implement quality control measures to ensure high standards. Provide technical support and guidance to junior team members. Ensure compliance with industry regulations and standards. Job Requirements Bachelor's degree in Mec...

ORGANISATIONAL OVERVIEW 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 Acts process owner of all Global studies ETMF and PDMS Quality review of CTM documents Low risk & repetitive EXPERIENCE Fresher EDUCATIONAL QUALIFICATION Fresher - B.Pharm/ M.Sc

ORGANISATIONAL OVERVIEW 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 SAS Programming for CDISC deliverables (SDTM, ADaM, define.xml) SAS Programing for Data Analytics & TLFs Teamwork, Resource management training & quality improvisation steps EXPERIENCE Fresher cadidates with > 80% scores in SAS certifica...

ORGANISATIONAL OVERVIEW 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 To determine whether all trial related activities were conducted, data recorded, analyzed and reported accurately & in compliance to all applicable Regulatory requirements, Organizational requirements (Policy, Procedures and processes) a...

The Role The Research Associate/ Executive/ Analyst for the Small Molecule Bioanalytical Laboratory is a technical role responsible for conducting BA/BE studies in the laboratory. Job responsibilities include performing critical method development and validation programs, technical and regulatory compliance of all studies. This role requires an individual with a robust background in pharmaceutics, or other related life sciences, coupled with extensive experience in the bioanalytical field, particularly within small molecule bioanalysis. This role demands an individual with a strong commitment to compliance, integrity, and excellence in bioanalytical research, particularly in small molecule a...

for Risk & Compliance New Associate Position Title:Risk & Compliance New Associate CL -13 Location: Bengaluru Employment Type: Full Time Must have skills : Risk & Compliance Good to have skills : Compliance About CF/S&C Corporate Functions include Human Resources, Finance, Legal, Marketing Communications, and Workplace Solutionsthat power Accenture's people across industries and functions to keep our business leading in the New. Join the heart and soul of Accenture, partnering with our extraordinary people to bring innovation into every organization. About Accenture: Combining unmatched experience and specialized skills across more than 40 industries, the company offers Strategy and Consulti...

Join Clario s industry-leading Digital Physiology team as a Principal Statistical Programmer, where your expertise will drive innovation in clinical research. This is a unique opportunity to lead advanced statistical programming for cardiac safety trials, shaping the future of digital health through cutting-edge data science and global collaboration. What we offer Competitive compensation + shift allowances Attractive benefits (security, flexibility, support and well-being) Engaging employee programs Technology for hybrid working and great onsite facilities What youll be doing Statistical Programming & Data Standards Lead and coordinate all statistical programming activities for cardiac safe...

Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years What would you do? Experience working in Client On-boarding, Account Maintenance, Customer Identification Program (CIP) and Know Your Customer (KYC) processes. Conducting PEPs (Politically Exposed Persons) screening and adverse media checks Proven analytical skills, problem solving ability, and a control mentality paired with meticulous attention to detail. Aptitude for building relationships and ability to communicate complex issues to a wide array of internal clients with differing levels of product experience. Self-motivated...

Job Overview/Summary : Join GSKs dynamic team to lead the AI product vision and strategy, driving innovative solutions that align with our R&D goals in target choice, patient identification, molecule design and clinical trial effectiveness. Motivate and guide a cross-functional team to meet milestones. Collaborate with experts to develop high-quality simulation modeling and analytical solutions. Shape the future of AI at GSK by establishing clear roadmaps, promoting adoption, and delivering industry-leading products. Responsibilities: Take the lead in identifying ambitious opportunities and shaping AI product vision, strategy, and roadmaps in alignment with GSKs R&D goals. Drive innovation b...

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