Clinical Research Associate
1 week ago
Roles & ResponsibilitiesYou will be responsible to monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols under supervision of Clinical Operations Manager/ Clinical Research Specialist.You will be responsible to perform study site feasibility, qualification, initiation, monitoring and close-out activities (remotely/ on-site) under supervision in line with study specific project management/ sponsor oversight plan and apply judgment and knowledge to independently resolve site issues, questions, and concerns.You will support Clinical Operations Manager/ Clinical Research Specialist to prepare for project kick-off/ investigator’s meeting.You will be desirous to build and maintain relationships with investigators and site staff.You will be responsible to address and resolve issues at sites, including the need for additional training, potential deficiencies in documentation and communication.You will responsible for documentations under supervision and ensure maintenance of Trial Master File/ Sponsor Oversight File in line with study specific project management/ sponsor oversight plan.You will Support study sites in making Ethics Committee submissions under supervision in
line with study specific project management/ sponsor oversight plan.You will be responsible to review & follow-up on site payments.You will assist with data query resolution process for site, Clinical Research organisation (CRO) and Sponsors along with Clinical Data Management in line with study specific projectmanagement/ sponsor oversight plan.You will be responsible to work collaboratively with the study teams with the review, revision and writing of protocols, Case Report Forms (CRF) and other required documents for clinical research studies.
QualificationsEducational qualification:
Master degree in pharmacy/ life science/Biology/Biotechnology/ Biochemistry/Diploma in Clinical ResearchMinimum work experience:
2 - 5 years of research experienceSkills & attributes:Technical SkillsExperience in Clinical Trial operations.Proficiency in conducting Market research and analysis.Knowledge of regulatory requirements and guidelines such as Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.Ability to evaluate medical research data and proficient knowledge of medical terminologyProficiency in using EDC systems for data collection and management in clinical trials.Understanding of pharmacovigilance processes.Strong MS office Skills.Behavioral
SkillsExcellent communication, negotiation, and interpersonal skills.Excellent project management skills.Strong analytical and problem-solving abilities with a keen eye for detail.Result oriented and passionate about delivering value.
Additional InformationAbout the DepartmentIntegrated Product Development OrganisationWe integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosagesOur product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.Benefits OfferedAt Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.Our Work CultureAsk any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.For more details, please visit our career website at
-
Clinical Research Associate
3 months ago
Hyderabad, India Mercury Connections Full time**Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe.** **Salary**: ₹500,000.00 - ₹600,000.00 per year **Benefits**: - Health insurance Schedule: - Day...
-
Clinical Research Associate
1 week ago
hyderabad, India Dr Reddy's Laboratories Limited Full timeJob DescriptionJob Summary We are seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other...
-
Clinical Research associate-Reputed Medical
3 months ago
Hyderabad, India Seven Consultancy Full timeJOB DETAILS1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics committee...
-
Clinical Research associate-Reputed Medical
4 months ago
hyderabad, India Seven Consultancy Full timeJOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...
-
Clinical Research associate-Reputed Medical
2 days ago
hyderabad, India Seven Consultancy Full timeJOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee. 2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics...
-
Research Associate
4 weeks ago
Hyderabad, Telangana, India Makrocare Full timeResearch Associate **Role and Responsibilities**: - ** Comprehensive Research**: Perform detailed secondary research to create comprehensive profiles of Food, Nutritional, Pharmaceutical products, including drugs, clinical studies, and medical devices. - ** Data Capture**: Collect and analyze data from a variety of sources such as press releases, annual...
-
hyderabad, India Seven Consultancy Full timeJOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...
-
hyderabad, India Seven Consultancy Full timeJOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee. 2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics...
-
Clinical Research Coordinator
2 weeks ago
hyderabad, India Continental Hospitals Full timeWe're looking for a highly skilled Clinical Research Coordinator with a strong background in managing clinical trials. The ideal candidate will have 5+ years of experience in domestic and international trials, ensuring compliance with statutory guidelines and regulations.Key Responsibilities:Coordinate clinical trials from initiation to closure.Manage study...
-
Clinical Research Coordinator
2 weeks ago
Hyderabad, India Continental Hospitals Full timeWe're looking for a highly skilled Clinical Research Coordinator with a strong background in managing clinical trials. The ideal candidate will have 5+ years of experience in domestic and international trials, ensuring compliance with statutory guidelines and regulations. Key Responsibilities: Coordinate clinical trials from initiation to closure. ...
-
Clinical Research Coordinator
2 weeks ago
Hyderabad, India Continental Hospitals Full timeWe're looking for a highly skilled Clinical Research Coordinator with a strong background in managing clinical trials. The ideal candidate will have 5+ years of experience in domestic and international trials, ensuring compliance with statutory guidelines and regulations. Key Responsibilities: Coordinate clinical trials from initiation to closure. Manage...
-
Clinical Research Coordinator
3 weeks ago
Hyderabad, India Continental Hospitals Full timeWe're looking for a highly skilled Clinical Research Coordinator with a strong background in managing clinical trials. The ideal candidate will have 5+ years of experience in domestic and international trials, ensuring compliance with statutory guidelines and regulations.Key Responsibilities:Coordinate clinical trials from initiation to closure.Manage study...
-
Clinical Research Coordinator
1 week ago
Banjara Hills, Hyderabad, Telangana, India Basavatarakam Indo American Cancer Hospital & Research Institute Full time**For further details please contact: -**: **Telephone No**:040-2355 1235** Extn: 2266**: **Name of the Position**: Clinical Research Coordinator (CRC) **Department**:Clinical Trials **Qualifications**: Dpharm / B. Pharm / M. Pharm / Pharm D / Pharmaceutical Biotechnology etc. **Experience**: 1-2 years in hospital/ pharma industry **Salary**: As per the...
-
Clinical Research Associate
4 months ago
Hyderabad, India Dr.Reddy's Full time) Act as DRL’s direct contact with assigned sites, assess and ensure overall integrity of study 2) Implementation and adherence to study protocol at clinical investigational sites, and resolve site issues. Escalate issues that were unresolved to COL/PL. 3) Build and maintain relationships with investigators and site staff. 4) Facilitate and support site...
-
Clinical Research Coordinator
4 months ago
Hyderabad, India EDEMERA GLOBAL PRIVATE LIMITED Full timeOverseeing the trouble-free running of clinical trials - Collecting data obtained from research, coding and analyzing it - Managing budgets set aside for research - Communicating with participants regarding study objectives - Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules - Liaising with laboratories...
-
Content Editor
3 months ago
Hyderabad, India Clarivate Full timeAssociate/Content Editor - Clinical Studies Team As an Associate/Content Editor in Clinical team, you will be responsible for actively seeking out information about Clinical Studies, analyze, cross reference, and update all new or previously updated information in the clinical records from various sources, which includes scientific meetings, conferences,...
-
Research Associate
4 weeks ago
Hyderabad, Telangana, India MAKRO Full time**Role and Responsibilities**: **Comprehensive Research**: Perform detailed secondary research to create comprehensive profiles of Food, Nutritional, Pharmaceutical products, including drugs, clinical studies, and medical devices. **Data Capture**: Collect and analyze data from a variety of sources such as press releases, annual reports, clinical trial...
-
Clinical Research Coordinator
4 months ago
Hyderabad, India NanoCare Health Services Private Limited Full time**Responsibilities** - Create and monitor efficacy of clinical algorithms to risk profile patients for various non-communicable diseases - Design, implement and measure effectiveness of scalable interventions to improve prescription compliance. Oversight of patients’ health under NanoHealth’s plan - Represent NanoHealth at domestic and international...
-
Clinical Sciences Expert
3 months ago
Hyderabad District, Telangana, India Novartis Full time7000 patients, 1200 clinical sites, 40 countries, 100+ clinical studies led by Novartis Clinical Sciences & Innovation (CS&I) last year. Who are we? We are Clinical Sciences and Innovation at Novartis. A dynamic group of Clinical Scientists who plan and execute early phase trials worldwide in general medicine. From First-in-Human to Proof-of-Concept and...
-
Associate Clinical Trial Leader
4 months ago
hyderabad, India Novartis Full timeYour responsibilities include, but are not limited to:May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of...
