3711 Clinical Research Jobs - Page 43

Roles and Responsibility Assist in the development and implementation of new sample collection protocols. Collaborate with cross-functional teams to ensure seamless sample collection processes. Develop and maintain relationships with key stakeholders, including healthcare professionals and patients. Conduct site visits to monitor and evaluate sample collection practices. Analyze data to identify trends and areas for improvement in sample collection. Provide training and support to junior staff members on sample collection best practices. Job Requirements Bachelor's degree in any discipline; relevant certifications or training programs are an asset. Proven experience in sample collection, pre...

Description We are seeking a skilled Interventional Cardiologist to join our dynamic team. The ideal candidate will have 5-10 years of experience in performing interventional cardiology procedures and a strong background in managing cardiovascular diseases. This role requires a dedicated professional who is passionate about providing high-quality patient care and advancing their skills in a fast-paced clinical environment. Location - Adoor(Kerala) Responsibilities Performing diagnostic and interventional procedures related to cardiovascular diseases. Evaluating patients medical histories and conducting physical examinations. Interpreting diagnostic tests and imaging studies such as echocardi...

Job Summary The IPDRG Medical Coder is responsible for assigning accurate codes to inpatient medical records, ensuring compliance with coding standards and contributing to the efficiency of healthcare processes. Key Responsibilities Assign IPDRG codes to inpatient medical records based on established guidelines and regulations. Review and interpret clinical documentation to ensure accurate coding. Collaborate with healthcare professionals to resolve documentation discrepancies. Meet coding accuracy and productivity targets. Stay informed about updates to coding standards and practices. Required Qualifications Certification: Valid CPC (Certified Professional Coder), CCS (Certified Coding Spec...

We are looking for a highly motivated and enthusiastic individual to join our team as a Trainee in Imaging Services at Vijaya Diagnostic Centre Limited. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Assist in the operation and maintenance of imaging equipment. Prepare patient samples for imaging procedures. Operate imaging equipment according to established protocols. Analyze images to identify potential health issues. Maintain accurate records of imaging results. Collaborate with healthcare professionals to provide excellent patient care. Job Requirements Strong understanding of biotechnology, pharmaceuticals, and clinical research principles. Ability to ...

We are looking for a highly motivated and enthusiastic individual to join our team as a Trainee in Imaging Services at Vijaya Diagnostic Centre Limited. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Assist in the operation and maintenance of imaging equipment. Prepare patient samples for imaging procedures. Operate imaging equipment according to established protocols. Analyze images to identify potential health issues. Maintain accurate records of imaging results. Collaborate with healthcare professionals to provide excellent patient care. Job Requirements Strong understanding of biotechnology, pharmaceuticals, and clinical research principles. Ability to ...

Responsibilities: Prepare clinical study reports, protocols & newsletters Design medical affairs strategies Conduct literature reviews & ICH compliance checks Write scientific documents with CRF & KOL input Protocols, abstracts, posters, manuscripts Provident fund

Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with. The opp...

Assist in site selection, initiation, monitoring, and close-out visits. Ensure that clinical trials are conducted in accordance with protocols, SOPs, GCP, and regulatory requirements. Verify the accuracy and completeness of case report forms (CRFs) and source documents. Maintain essential documents in the Trial Master File (TMF). Assist in resolving data queries and discrepancies with the site staff. Support investigators and site staff in trial-related activities. Participate in project team meetings and training sessions. Prepare visit reports and follow-up letters. Maintain regular communication with study sites to ensure compliance and timely data entry.

Job Summary Research Associate responsible for supporting clinical and academic research through data collection, analysis, documentation, and report preparation. Involves coordination with investigators, maintaining research records, ensuring compliance, and contributing to publications and presentations. Key Responsibilities Writing research publications - Researching, writing, editing, and fact- checking content, while ensuring it meets the publication standards, deadlines and editorial guidelines. Assist in planning, organizing, and coordinating clinical and academic research studies. Collect, analyse, and interpret data using appropriate statistical tools. Maintain accurate research doc...

As a Medical Annotations trainer, we are looking for a doctor (MBBS) who has: Good clinical knowledge 2 plus years of experience in various clinical departments of a large hospital Awareness of different medical coding systems like SNOMED, RxNorm, CPT, ICD 10, LOINC. Has experience in a training role and has the following competencies: A. Training needs assessment through: 1. Review and assessment of the project objectives 2. Evaluation of skillset and knowledge base of new annotators 3. Evaluation of performance of annotators 4. Review of client and management feedback B. Creation of training programs C. Preparation of learning materials for training programs D. Develop onboarding programs ...

Roles and Responsibility Assist in operating X-ray equipment and other medical imaging devices. Prepare patients for X-ray procedures and ensure proper patient positioning. Maintain accurate records of X-ray images and results. Collaborate with healthcare professionals to provide high-quality patient care. Develop and implement new techniques to improve X-ray image quality. Participate in ongoing education and training to stay current with latest technologies and techniques. Job Requirements Strong knowledge of X-ray principles and practices. Ability to work effectively in a fast-paced environment. Excellent communication and interpersonal skills. Ability to maintain confidentiality and hand...

We are looking for a highly skilled and experienced Assistant to join our team at Vijaya Diagnostic Centre Limited. The ideal candidate will have 1-3 years of experience in sample collection. Roles and Responsibility Assist in the development and implementation of new sample collection protocols. Collaborate with cross-functional teams to ensure seamless sample collection processes. Develop and maintain relationships with key stakeholders, including healthcare professionals and patients. Conduct site visits to monitor and evaluate sample collection practices. Analyze data to identify trends and areas for improvement in sample collection. Provide training and support to junior staff members o...

We are looking for a highly motivated and dedicated individual to join our team as an Assistant in Imaging Services at Vijaya Diagnostic Centre Limited. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Assist in the operation and maintenance of imaging equipment. Prepare patient samples and materials for imaging procedures. Monitor patient vital signs and reactions during imaging procedures. Maintain accurate records of imaging results and patient information. Collaborate with healthcare professionals to provide high-quality patient care. Participate in quality control and quality assurance activities to ensure excellence in imaging services. Job Requirements...

Position Summary: The Manager, Payments is responsible for ensuring execution of the end-to-end clinical site payments process for an assigned country or region. The Manager will work closely with other teams within Contract & Centralized Services (CCS) and within the broader Global Clinical Operations (GCO) organization to ensure timely, accurate, and compliant payments to clinical investigator sites for clinical trial related activities. Principal Responsibilities: Process Oversee end-to-end payment process, ensuring accuracy, compliance with company policies and regulatory requirements, and adherence to contractual timelines Work as part of a global team, collaborating with other regional...

Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Essential Functions To Prioritize and complete the assigned trainings on time Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements. To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information determining ...

Role requirements Analyze, prepare and process accounting entries; analyze, maintain and reconcile general ledger accounts. Prepare profit and loss, income and balance sheet statements. Maintain inter-company accounting records and reconciliations. Provide records of assets, liabilities and other financial transactions. Prepare ad hoc reports for internal and inter-departmental use. Prepare reports and analyze for use in the annual external audit. Ensure accuracy and compliance with all accounting regulations and Sarbanes Oxley requirements. Check that appropriate approvals are obtained for accounting purposes. Provide recommendations to improve existing processes and suggest alternatives wh...

At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Key responsibilities: Core scientific member of cross-functional franchise team and a disease area expert, responsible for scientific enablement of respective business cluster C...

Biostatistician Responsible for statistical tasks in clinical trials including design, analysis, reporting, SAPs, and meta-analyses. Provide consultation, ensure quality deliverables, support publications, and comply with GCP/regulatory guidelines.

Regulatory Intern / Graduate Trainee This role involves assisting in the preparation and review of clinical trial documentation, maintaining regulatory databases, and researching regulatory guidelines for medical devices. The candidate will help in preparing documents for regulatory approvals in India and may take on additional responsibilities as assigned. Ideal candidates are freshers in Life Sciences, Pharmacy, Biomedical Engineering, or related fields , with strong attention to detail, communication skills, and proficiency in Microsoft Office. The role offers hands-on experience in regulatory affairs, industry exposure, and networking opportunities in the medical device sector. RD Intern...

Junior Assistant - Production - Serigen Mediproducts Private Limited About Us: Serigen is an innovation-driven tissue generation products company founded with the vision to become a global leader in biomedical devices. We are seeking a proactive Junior Assistant to support Manager and the team in various Production Activities. Key Responsibilities: Managing and handling of all instruments Maintenance of all equipment for smooth operation of production activity Helping team in cutting, packaging and sealing of products Helping team for dispatch related all activity Any documentation activity related to production activity mainly for instruments and handle production processes Any other respon...

Job Type: Full time (Work from Office) About Us: Serigen is an innovation-driven tissue generation products company founded with the vision to become a global leader in biomedical devices. We are seeking a proactive Junior Assistant to support Manager and the team in various Production activities. Key Responsibilities: Executing of regular production activity for wound care products Perform calibration activities of all production equipment s Regular data entry compliance to ISO 13485 related to all production activity Any other responsibility given by reporting officer Candidate s Profile: BSC Chemistry/ biochemistry/ biotechnology Experience: 0-2 years Handling of instruments like centrifu...

PURPOSE & CONTEXT: As a professional at Unilever, you ll enjoy the responsibility to lead change putting your fresh thinking into action. We ll equip you with the tools you need to do the job and more, enabling you to use your unique perspective to grow beyond limits and make a positive impact on the world, our business, and our people. Find your purpose at Unilever. You will lead innovations, big and small, that will make our business win and grow. You will learn from brilliant business leaders and colleagues in a truly global and diverse culture to ultimately become a better you. If you are passionate about creating a positive impact to our people, planet, and business by bringing science ...

Regulatory - Manager - Serigen Mediproducts Private Limited About Us: Serigen is an innovation-driven tissue generation products company founded with the vision to become a global leader in biomedical devices. We are seeking a proactive and organized Manager to support directors and the team in ensuring compliance to the regulatory requirements related to the products of Serigen and the implementation of QMS (ISO 13485) Key Responsibilities: Developing the regulatory strategy for various products in India and other global markets Preparing and submitting documentation required for regulatory approvals Co-ordinating and communicating with regulatory agencies for seeking various regulatory app...

Company Description . Job Description To enable AbbVie s emergence as a world class RD organization, the Site Management and Monitoring (SMM) Country/District COM plays a leadership role accountable for driving the business of SMM within a Country/District(s) by providing oversight and direction to SMM staff; accountable for the on time, within budget and quality delivery of the clinical studies. Promotes best practice; identifies infrastructural improvements and implements action plan to ensure Clinical Field Operations (CFO) and business objectives are successfully met; ensures alignment of local activities with regional/global initiatives. The role reports into the Site MM Leadership and ...

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...