Average salary: Rs1,603,727 /yearly
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...Job Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The...
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines and company SOPs.
Assist in site qualification initiation and monitoring visits.
Review and track clinical trial documentation...
...Clinical associates may be called upon to perform an EKG or to assist a nurse or doctor with a procedure . They provide patient care needs, including phlebotomy assistance, and collect updated and amended regulatory documents in collaboration with the CRA.
Assist attending...
...Execute trial TMF QC activities in accordance with TCO portfolio and Clinical Operations Transition Decision Point (TDP) and Clinical Study... ..., work streams and governances. May perform Clinical Project Associate (CPA) tasks as assigned
Commitment to Diversity & Inclusion...
...We are hiring for CRAII and Senior CRAs across India.
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...
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements...
...and guidelines, and Takeda requirements
ACCOUNTABILITIES:
Lead the development of the study specific eTMF plans for assigned clinical studies.
Perform quality control of documents submitted to the eTMF using the established acceptable criteria
Ensure clinical...
...(Provides troubleshooting) -Coaching and technical training as technical expert or leader.
Act as mentor for junior and senior associates.
Understand resource constraints and identify and implement cost saving opportunities -Show positive work ethics and influences others...
...About the job
Summary
Monitors patient data study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into...
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
With...
Remote job
...Job Description
We're looking for a proactive and highly communicative clinical research professional, pivotal in critically analyzing and summarizing clinical literature to provide valuable insights. Collaborating with cross-functional teams, you will contribute to the...
...Ensure 100% adherence to monitoring and study plan
Support clinical quality in managing CAPAs and other study audit observations... ...years’ experience in clinical trials industry as Clinical Research Associate
Good working knowledge of GCP and local clinical trial rules...
...Job Description
JOB TITLE : Associate Director- Clinical Regulatory Writing
CAREER LEVEL: E
Lead the way for a new breed of solutions-oriented Regulators
Champion a new approach to Regulatory that supports quick decision-making and balanced risk-taking. Curious...
Compilation and publishing of clinical and safety documents
Coordinate and ensure quality of CTR appendix material
Perform electronic quality control (eQC) of applicable clinical and safety documents
Ensure quality deliverables of Non-clinical reports
To have...
...Clinical Data Management (CDM)
Clinical Data Managers (CDMs) are responsible for ensuring the accuracy, integrity, and completeness of data collected in clinical trials. They work closely with clinical investigators, statisticians, and other members of the clinical trial...
...Job Title : Clinic Acquisition Associate - Dental SaaS Sales Company : RCMS- India Location : Kerala, India Compensation : Competitive base salary - Performance-based incentives - Fuel allowances for field work About Us : RCMS- India is revolutionizing the way dental practices...
...As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.
Key...
...Associate Clinical Data Manager
SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner...
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up and equip trial sites with necessary materials and equipment.
Train site staff on study procedures and data collection methods...
...We are looking for an organized, flexible Clinical Research Associate to oversee clinical trials. The Clinical Research Associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials....
