{"id":9941,"date":"2025-02-28T15:28:08","date_gmt":"2025-02-28T09:58:08","guid":{"rendered":"https:\/\/translumina.com\/in\/?post_type=awsm_job_openings&#038;p=9941"},"modified":"2025-07-15T16:56:02","modified_gmt":"2025-07-15T11:26:02","slug":"clinical-research-associate-cra","status":"publish","type":"awsm_job_openings","link":"https:\/\/translumina.com\/in\/jobs\/clinical-research-associate-cra\/","title":{"rendered":"Clinical Research Associate (CRA)"},"content":{"rendered":"<p><strong>Experience:<\/strong> Min. 3 Years<br \/>\n<strong>Preferred:<\/strong> Healthcare Industry<br \/>\n<strong>CTC:<\/strong> As per industry standards.<\/p>\n<p><strong>Key Responsibilities:<\/strong><\/p>\n<ul>\n<li>Will develop the outline trial protocols and manage Investigational Product (IP) and trial materials.<\/li>\n<li>Will manage multiple aspects of subjects&#8217; welfare.<\/li>\n<li>project coordination with CRO\u2019s, carry monitoring visit at CRO to manage study logistics.<\/li>\n<li>Will conduct regular site visits, generate, and distribute internal and external newsletters, prepare final reports and liaison with interested parties regarding all trial aspects.<\/li>\n<li>Identify, evaluate, and establish trial sites, and ensure the completion of trial.<\/li>\n<li>To train site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.<\/li>\n<li>Liaison with ethics committee regarding rights, safety, and well-being of trial subjects.<\/li>\n<li>Overseeing and documenting IP dispensing, inventory, and reconciliation.<\/li>\n<li>Protecting subjects\u2019 confidentiality, updating their information, and verifying IP has been dispensed and administered according to the protocol.<\/li>\n<li>Conducting regular site visits, coordinating project meetings, and writing visit reports.<\/li>\n<li>Implementing action plans for sites not meeting expectations.<\/li>\n<li>Liaising with regulatory authorities.<\/li>\n<li>Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines.<\/li>\n<li>Other tasks and responsibilities as needed.<\/li>\n<li>Collaborative approach of working with Sales &amp; Marketing team for initiating projects.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>Additional Skills:<\/strong><\/p>\n<ul>\n<li>Bachelor\u2019s degree in Biological Science or a related field<\/li>\n<li>Computer proficiency<\/li>\n<li>Excellent numerical, written, and verbal communication skills<\/li>\n<li>Excellent research skills and attention to detail<\/li>\n<li>Sharp analytical and critical thinking<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Experience: Min. 3 Years Preferred: Healthcare Industry CTC: As per industry standards. Key Responsibilities: Will develop the outline trial protocols and manage Investigational Product (IP) and trial materials. Will manage multiple aspects of subjects&#8217; welfare. project coordination with CRO\u2019s, carry monitoring visit at CRO to manage study logistics. Will conduct regular site visits, generate, and [&hellip;]<\/p>\n","protected":false},"author":2,"template":"","meta":{"_acf_changed":false},"class_list":["post-9941","awsm_job_openings","type-awsm_job_openings","status-publish","hentry","job-type-full-time","job-location-delhi-ncr"],"acf":[],"_links":{"self":[{"href":"https:\/\/translumina.com\/in\/wp-json\/wp\/v2\/awsm_job_openings\/9941","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/translumina.com\/in\/wp-json\/wp\/v2\/awsm_job_openings"}],"about":[{"href":"https:\/\/translumina.com\/in\/wp-json\/wp\/v2\/types\/awsm_job_openings"}],"author":[{"embeddable":true,"href":"https:\/\/translumina.com\/in\/wp-json\/wp\/v2\/users\/2"}],"wp:attachment":[{"href":"https:\/\/translumina.com\/in\/wp-json\/wp\/v2\/media?parent=9941"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}