6710 Clinical Research Jobs - Page 36

Join us as a Trade & Transaction Reporting Manager Well look to you to provide oversight on daily trade and transaction reporting processes, making sure that they adhere to the control framework and comply with regulatory obligations Youll provide input into regulatory reporting initiatives, through your expertise and knowledge of regulations, data analysis and issue remediation As a key member of our team, youll enjoy extensive collaboration and can expect great visibility for you and your work We're offering this role at vice president level What you'll do As a Trade & Transaction Reporting Manager, youll be operating a robust oversight model of trade and transaction submissions to support...

Role & responsibilities: Minimum 2 to 5 years of Experience with Clinical Data Management practices and relational database management software systems preferred. Strong background in conducting CDM activities. Must have in-depth understanding of the current activities involved in the present organization and good understanding of all the phases set up, conduct & closeout.

We are looking for an Associate STEM Content Analyst to join our CDDI Chemistry team in Chennai (India). This is an amazing opportunity to work on content analysis for our Cortellis Drug Discovery Intelligence (CDDI) product. The team consists of 17 members based across Chennai, Hyderabad, Bangalore and Barcelona (Spain) and this role reports to the Chemistry Team Manager. We have a great skill set in Chemistry, Pharamacology, Medicinal chemistry, Synthesis andcomplementary skill sets to address challenges in drug discovery, including new chemical drugs identification, curation of drugs and formulations. We would love to speak with you if you have an understanding of chemical drug products. ...

We are looking for a Senior Solutions Analyst to join our Solutions Analyst Team This is an amazing opportunity to work on LS&H Research & Development Business Unit on LS&H production processes improving the timeliness, quality of data release as well as the editorial user experience The team consists of 7 People and is reporting to the Solutions Analyst Manager We have great skill set in different Life Science production products, and we would love to speak with you if you have skills or interests for the same About You experience, education, skills, and accomplishments Bachelors Degree or Equivalent Minimum of 5 Years of Relevant Experience Provide guidance to stakeholders in the developme...

Greetings from Wipro!! We are inviting applicant for Walk-in Drive-in Pune Location for Pharmacovigilance Experience- 1 to 2 years Qualification- B. Pharm/ M. Pharm with valid Pharma license Only the qualifications mentioned are eligible Candidate should have excellent Communication in English Should be ready for Rotational shifts Should have excellent knowledge of Pharmacovigilance Should be ready to work from office Should be ready to relocate to Pune Walk In Date- 4-Nov -25 Time to Report- 10.00 A.M- 12.30 P.M Documents to carry- Update CV & original govt. ID Card. Should mention at the top of the CV the source of information about the walk-In Walk in Address- Unit 2, Plot No 31, Hinjewad...

Research Assistant (Jewellery) Mumbai & New Delhi Key Responsibilities: Working on machines in Labs for Diamond & Jewellery Experience: Min 1 years of experience of working on machines in Labs for Diamond & Jewellery Precise in working and handling Diamonds & Jewellery Required Skills: Flexible in working hours Smart and presentable Good communication skills Can talk, read & communicate in English Open for Multitasking work culture Education & Certifications: Min HSC and Graduate Work Environment : Able to travel to multiple locations as and when required May occasionally be required to work overtime to meet deadlines.

Site Name: Bengaluru Luxor North Tower Posted Date: Oct 29 2025 Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. We're uniting science, technology, and talent to get...

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining impossible. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Medical Advisor POSITION PURPOSE: The position is responsible for the medical and scientific support, including technical ad...

About JAQA World Foundation : JAQA World Foundation is dedicated to advancing mental health care by integrating clinical excellence with innovative, evidence-based and holistic approaches. We collaborate with mental health professionals to offer cutting-edge community programs, telepsychiatry, and wellness initiatives with a focus on accessibility and impact. Role Overview: We are seeking experienced mental health doctors and psychiatrists to join us as consultants. In this role, you will provide expert psychiatric evaluations, therapeutic interventions, and guidance on digital and community mental health projects on a flexible, consultancy basis. Key Responsibilities: Provide psychiatric co...

At Allucent, you will be a Sr. Clinical Research Associate Contractor (Sr.CRA) responsible for independently controlling and monitoring investigational sites, ensuring clinical studies are conducted according to trial protocols and in compliance with SOPs, regulations, and Good Clinical Practice principles. **Key Responsibilities:** - Govern highest quality standards for trial monitoring activities. - Conduct all study tasks in compliance with quality standards while maintaining efficiency. - Monitor activities at clinical study sites to ensure adherence to protocols, ICH, GCP, SOPs, and regulations. - Prepare and submit quality Site Visits Reports and Contact reports. - Maintain and update ...

Job Description You are eligible to apply for this job if you have just passed the University/National Board Examinations. Qualification Required - Candidates who have just passed the University/National Board Examinations,

As a Senior Quality Auditor at Precision, you will play a crucial role in ensuring compliance with regulations and company procedures for clinical projects. Your responsibilities will include: - Supporting the Quality Management System by managing SOPs, training, and CAPA - Processing and maintaining documentation for controlled documents - Developing and administering training for employees and consultants - Hosting client/sponsor audits and supporting regulatory inspections - Coordinating and conducting assessments of vendors, including vendor audits - Conducting internal audits of quality systems, investigator site audits, and trial master file audits - Participating in computer systems v...

Role Overview: Working at Bristol Myers Squibb is a unique experience where challenging and meaningful work happens every day, transforming the lives of patients and the careers of employees. You will have the opportunity to grow and thrive through unparalleled opportunities while being part of high-achieving teams. Key Responsibilities: - Conduct site qualification, initiation, routine monitoring, and close-out visits across all trial phases - Verify data integrity within electronic systems and paper records to ensure data accessibility, completeness, and accuracy - Monitor site adherence to ICH GCP and local regulations, ensuring data integrity and patient safety - Cultivate effective rela...

Role Overview: As a Lead NIS Excellence Associate at GSK, you will have the opportunity to drive excellence in non-interventional studies (NIS) and contribute to making a meaningful impact on healthcare. Your role will involve leading and managing NIS processes while ensuring compliance with regulatory requirements and internal standards. Collaboration with global and local teams, development of process documentation, and providing guidance and training to stakeholders will be key responsibilities. This position offers opportunities for professional growth, innovation, and alignment with GSK's mission to unite science, technology, and talent to advance disease prevention and treatment. Key R...

Company Description The CPA Institute is a premier educational institution dedicated to excellence in Pharmaceuticals, Clinical Research, Medical Coding, and Life Sciences, with 12 years of experience. We empower professionals with the knowledge and skills needed to thrive in healthcare and life sciences sectors. Our programs are designed to prepare students for competitive examinations, such as the Graduate Pharmacy Aptitude Test (GPAT), National Institute of Pharmaceutical Education and Research Joint Entrance Exam (NIPER JEE), and the Government Pharmacist Exam. Role Description This is a full-time, on-site role located in Lucknow for a RRB Pharmacist Prep Trainee. The RRB Pharmacist Prep...

Brief Description About The Project Interaction with Patients, Sponsor/CRO, IEC, Lab staff and other departments in the institution and conduct the study according to ICH GCP Guidelines, SOPs and study protocol guidelines and act as the main line of communication between patients, Investigators and CROs in study conduct activities. Assist in Feasibility questionnaires, Coordinate in pre-site selection visit, site initiation visit. Assist the Principal Investigator and Co investigators in screening of subjects by maintaining and updating the list of potentially eligible patients for the ongoing studies. Clinical Research Co-ordinator No. of Vacancy: Two Preferred Qualifications: Degree with l...

SUMMARY About Client Client is a leading healthcare services organization that partners with healthcare providers to improve clinical, financial, and operational outcomes. With a focus on technology-enabled solutions and process excellence, delivers services such as medical coding, revenue cycle management, clinical documentation, and patient engagement. The company operates globally, with a strong presence in India and the United States, supporting some of the largest healthcare groups and physician organizations. Job Title: Medical Coder Reporting To: Team Manager Designations Reporting to this Role: None Department: Medical Coding Location:Coimbatore Profile Description The role involves ...

SUMMARY About Client Client is a leading healthcare services organization that partners with healthcare providers to improve clinical, financial, and operational outcomes. With a focus on technology-enabled solutions and process excellence, delivers services such as medical coding, revenue cycle management, clinical documentation, and patient engagement. The company operates globally, with a strong presence in India and the United States, supporting some of the largest healthcare groups and physician organizations. Job Title: Medical Coder Reporting To: Team Manager Designations Reporting to this Role: None Department: Medical Coding Location: Mumbai Profile Description The role involves the...

Job Role: Biomedical Engineer / Technical Clinical Support Engineer Experience: 1+ Years Location: Coimbatore (On-site) Industry: Biomedical / Medical Devices Key Responsibilities: Provide technical and clinical support to clients on-site Analyze client requirements and convert them into effective technical solutions Manage post-sales support, documentation, and client feedback Collaborate with internal teams for project coordination and execution Participate in technical conferences, demos, and training sessions Qualification & Skills: B.E. / B.Tech in Biomedical Engineering. Strong understanding of Human Anatomy and Clinical Research Excellent communication and client-handling abilities Kn...

This role involves the creation and validation of clinical study datasets, ensuring compliance with CDISC SDTM standards. The candidate will collaborate with cross-functional teams to support clinical data transfer.

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...

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, PHARMACY B.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry). 2020 -2024 passed out 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 analys...

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...

Role & responsibilities 1. Responsible for clinical trial medical science related activities like preparation of protocol, Informed consent form, CRF, other study related documents and SOPs in line with ICH GCP, Indian and global regulatory. 2. Conduct relevant literature search for required for protocol and manuscript writing. 3. Ensures that medical writing deliverables conform to International Conference on Harmonization (ICH) and other relevant regulatory guidelines. 4. Ensure to follow all clinical and regulatory guidelines, processes and systems for medical science activities and ensure compliance to internal medical writing SOPs for Clinical trial. 5. Compiles, writes and edits medica...

As a Clinical Project Manager at Clario's Medical Imaging team in Bengaluru, India, you will be part of a legacy with over 30 years of expertise in providing seamless, secure, and compliant medical imaging solutions that enhance clinical trials. You will have the opportunity to contribute to ambitious goals and a clear vision for the future. **Role Overview:** You will be responsible for: - Identifying project guidelines and communication needs by reviewing study requirements and collaborating with key stakeholders - Defining project plans, establishing project reporting schedules, and providing project updates to relevant parties - Performing project analysis and management by identifying c...