Senior Medical Monitor, Contractor Biorasi

5.0 - 7.0 years

0 Lacs

India

On-site

We are Growing ! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization. Biorasi is looking for top performers who are as passionate about clinical research as we are – clinical trial veterans and industry newcomers who will thrive in our fast-paced environment and help us drive new therapies to patients. Here is your chance to become a vital part of a growing global company in the expanding clinical research industry. Your role: Act as a primary or backup Medical Monitor for the assigned clinical studies. Oversee multiple studies, contribute to the regulatory submissions (INDs, etc.) Responsible for providing protocol/therapeutic training to the study team, as required. Provide medical expertise to investigators and study team and advise on medical related questions. Perform eligibility review of the study subjects, as required. Lead in medical review, assessment, and interpretation of clinical and safety data to ensure that the data are correct and presented with the appropriate medical interpretation. Escalate any critical safety concerns to the study team and Sponsor, and coordinate between sites and study team/Sponsor. Responsible for identifying, reviewing and confirming protocol deviation classification Lead the Medical Monitoring and Protocol deviation project meetings, participate in any other Sponsor calls, if required. Work closely with Safety and Pharmacovigilance team to provide medical input into safety reports including, SAE narratives and analysis of similar events, periodic safety reports. Responsible for the review of individual data with SAEs and potentially clinically important laboratory test results or vital sign abnormalities and escalate issues to the Sponsor as needed. Assist in medical and scientific review of deliverables such as TLFs and CSR. Lead in developing and maintaining SOPs, Templates, and study plans Participate in the review of the design and conduct of clinical trials including the development and review of protocols and amendments. Assist in incorporating medical strategy into study feasibility required for new projects. Cooperate with program development and commercial teams to develop the medical strategy for the RFP for new projects. Participate and lead medical strategy section in the Bid Defense preparation and meetings. Responsible for Line Management of assigned team members in Medical and Scientific Affairs group. Support regulatory inspections and audits as needed. Your Profile: Medical degree, MD or its international equivalent. Active medical license Fluent English (oral and written). Proven 5-7 years’ work experience within the life science industry or related field Minimum 4 years’ experience with medical monitoring services Strong understanding of GCP/ICH guidelines and applicable regulatory requirements Excellent verbal, written communication and presentation skills. Critical Thinking and background medical and scientific research Strong Proficiency in using Microsoft Office Experience with safety databases (ARISg, Oracle Argus, etc.) and/or EDC system (Zelta, Medrio, Oracle Clinical, Medidata) Biorasi is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. Biorasi is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Posted 1 week ago

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Technical Project Manager Saama Technologies Inc

10.0 years

0 Lacs

Coimbatore

On-site

Saama - Technical Project Manager - JD Reports to: Program Manager Job Description ❖ Required / Must Have Skills ➢ Strong project management skills, including planning, execution, and risk management. ➢ Excellent communication and interpersonal skills, with the ability to effectively communicate with technical and non-technical audiences. ➢ Proven ability to lead and motivate cross-functional teams. ➢ Technical background or understanding of the technologies involved in the project. ➢ Minimum of 10 years of hands-on experience in Application programming. ➢ Ability to adapt to changing priorities and manage multiple projects simultaneously. ➢ Strong analytical, problem solving, troubleshooting & debugging skills. ➢ Knowledge on Python (otherwise Java or DotNet), SQL, Data Engineering, Data Analytics tools, AWS, etc. ❖ Good to have skills ➢ Good understanding of one or more of the following Clinical Systems EDC Systems such as Medidata Rave, Veeva EDC, Oracle Clinical, Medrio, InForm, etc., CTMS Systems such as Siebel CTMS, Medidata CTMS,Veeva CTMS, etc., IRT Systems such as YPRIME, Parexel Clinphone, etc., LAB Systems such as central Lab, local Labs etc., ➢ Good understanding of clinical trial domain & overall EDC study setup & reporting process.

Posted 2 weeks ago

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Technical Project Manager Saama

10.0 years

0 Lacs

Chennai, Tamil Nadu, India

On-site

Description Saama - Technical Project Manager - JD Reports to: Program Manager Job Description ❖ Required / Must Have Skills Strong project management skills, including planning, execution, and risk management. Excellent communication and interpersonal skills, with the ability to effectively communicate with technical and non-technical audiences. Proven ability to lead and motivate cross-functional teams. Technical background or understanding of the technologies involved in the project. Minimum of 10 years of hands-on experience in Application programming. Ability to adapt to changing priorities and manage multiple projects simultaneously. Strong analytical, problem solving, troubleshooting & debugging skills. Knowledge on Python (otherwise Java or DotNet), SQL, Data Engineering, Data Analytics tools, AWS, etc. ❖ Good to have skills Good understanding of one or more of the following Clinical Systems ■ EDC Systems such as Medidata Rave, Veeva EDC, Oracle Clinical, Medrio, InForm, etc., ■ CTMS Systems such as Siebel CTMS, Medidata CTMS,Veeva CTMS, etc., ■ IRT Systems such as YPRIME, Parexel Clinphone, etc., ■ LAB Systems such as central Lab, local Labs etc., Good understanding of clinical trial domain & overall EDC study setup & reporting process.

Posted 2 weeks ago

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