Opening for expirenced CRC or CRA to work as Clinical Research Associate @ ICON Clinical Research Ltd - Mumbai, Maharashtra
Skill: communication skills,Clinical Research,Associate;
Exp: 2-7 years; This is an opportunity to work for ICON Clinical Research. With a track record for successful analysis and extensive scientific publication, the ICON Clinical Research division delivers high-impact evidence that explores and demonstrates the value of pharmaceutical, biotechnology, consumer healthcare and medical device products in all global markets, with a focus on maximising return on investment.Our global team of experts provide a full spectrum of market-leading clinical Late Phase research, real-world studies, health economics and patient reported outcomes to support our clients product lifecycle, from early stage development, pricing and market access strategies, through regulatory and reimbursement approvals, labelling claims, and in-market support.We now seek to recruit a dedicated, hardworking Clinical Research Associate, to join our busy European team.Overview of the roleWorking independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required. Depending on your level of experience, you may assist in training and mentoring less experienced CRA s and/or manage CRAs working on international projects.
Role Requirements With a University degree in medicine, science, or equivalent you will have previous monitoring experience in medium d studies, including study start-up and close-out (for all roles above Entry Level). You should also have knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data. Fluent in English, as well as the local language, you will possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner. You should be able to produce accurate work to tight deadlines within a pressurised environment.
You must be available to travel at least 50 of the time (international and domestic -fly and drive) and should possess a valid driving licence.You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.
Click here to apply
Skill: communication skills,Clinical Research,Associate;
Exp: 2-7 years; This is an opportunity to work for ICON Clinical Research. With a track record for successful analysis and extensive scientific publication, the ICON Clinical Research division delivers high-impact evidence that explores and demonstrates the value of pharmaceutical, biotechnology, consumer healthcare and medical device products in all global markets, with a focus on maximising return on investment.Our global team of experts provide a full spectrum of market-leading clinical Late Phase research, real-world studies, health economics and patient reported outcomes to support our clients product lifecycle, from early stage development, pricing and market access strategies, through regulatory and reimbursement approvals, labelling claims, and in-market support.We now seek to recruit a dedicated, hardworking Clinical Research Associate, to join our busy European team.Overview of the roleWorking independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required. Depending on your level of experience, you may assist in training and mentoring less experienced CRA s and/or manage CRAs working on international projects.
Role Requirements With a University degree in medicine, science, or equivalent you will have previous monitoring experience in medium d studies, including study start-up and close-out (for all roles above Entry Level). You should also have knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data. Fluent in English, as well as the local language, you will possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner. You should be able to produce accurate work to tight deadlines within a pressurised environment.
You must be available to travel at least 50 of the time (international and domestic -fly and drive) and should possess a valid driving licence.You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.
Click here to apply
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