Careers

At Jeevan, we believe that "our strength is our workforce".
Jeevan offers challenging assignments, excellent working environment, professional development and opportunities to train, learn, and execute projects.

Advertisements for staffing in Global Medical Services at JSTL

Jeevan Scientific Technology Limited, a publicly traded CRO located in Hyderabad, is soliciting qualified applicants to apply for the following positions:

Clinical Project Manager

The clinical trial project manager will play a critical role on our team and be responsible for various aspects of Jeevan Scientificís clinical trials in Hyderabad, India. This is a critical role that requires self-motivated, proactive and experienced individual in Monitoring and Project Management skills.

This position will also work closely with a cross-functional team to ensure that clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH, GCP, regulatory guidelines, company goals, and budgets.

In this role you will assist with the preparation of protocols and case report forms, finalization of monitoring and data management, and ensure the seamless integration of the clinical research team in all necessary capacities.

Job functions / responsibilities:

  • Managing a clinical project team
  • Managing clinical research sites
  • Executing clinical protocols
  • Oversee proper collection of data
  • Liaison with the study sponsor for project related activities
  • Monitor ongoing compliance to study protocols, FDA regulations, and IRB requirements
  • Preparing accurate and timely project reports
  • Complete projects and tasks in a manner consistent with corporate objectives and meet study timelines and budget
  • Participate in Inspection/Audit readiness and CAPA

Requirements:

  • Bachelorís Degree and above in Pharmacy or other medical discipline
  • Minimum 9 years experience in the clinical research industry
  • Minimum 2 years project management experience managing teams and direct reports
  • Knowledge of Local and International regulatory requirements
  • Excellent written and verbal communication skills
  • May require travel up to 20% of time
Senior Clinical Research Associate

Job functions / responsibilities:

  • Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
  • Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
  • Managing sponsor generated queries
  • Taking responsibility for study cost effectiveness
  • Preparation and review of study documentation and feasibility studies for new proposals
  • Potential to assist in training and mentoring fellow CRAs

Qualifications and Skills:

  • University degree in medicine, science, or equivalent
  • Previous monitoring experience in medium sized studies, including study start-up and close-out
  • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
  • Excellent written and verbal communication
  • Ability to work to tight deadlines
  • Availability to travel at least 40% of the time
Clinical Research Associate

Job functions / responsibilities:

  • Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
  • Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
  • Managing sponsor generated queries
  • Taking responsibility for study cost effectiveness
  • Preparation and review of study documentation and feasibility studies for new proposals
  • Potential to assist in training and mentoring fellow CRAs

Requirements:

  • University degree in medicine, science, or equivalent
  • Previous monitoring experience in medium sized studies, including study start-up and close-out
  • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
  • Excellent written and verbal communication
  • Ability to work to tight deadlines
  • Availability to travel at least 60% of the time
Bioanalytical Research Associate

Job functions / responsibilities:

  • Must have 1 - 4 years experience in Bioanalytical Research
  • Sample Preparation in Bioanalytical Research using Biological samples
  • Expertise in Bioanalytical Method Development and Method Validation
  • Project Sample Analysis as per regulatory requirements.
  • Handling lab equipment's like Balance, pH meter, Centrifuge, SPE manifold, HPLC and / LC-MS/MS
  • Preparation and review of SOPs / Protocols / Reports.
  • Candidates must have M.Sc./M.Pharm/B.Pharm
  • No. of Positions - 10 Approx.
Clinical Research Physician

Job functions / responsibilities:

  • Perform screening of volunteers and oversee the screening procedure.
  • Conduct clinical phase feasibility for the projects received.
  • Evaluate the synopsis and provide inputs for designing clinical phase of the study.
  • Review clinical study protocols and provide inputs as required with in the timelines.
  • Identify Investigators for the conduct of clinical phase based on the protocol requirements.
  • Conduct site initiation visits, site monitoring visits and site close out visits for clinical studies.
  • Conduct site feasibilities as required for the prospective clinical studies.
  • Monitor Clinical phase of Bioequivalence/Phase I/Phase Il/Phase Ill studies, as needed.
  • Review adverse event and Serious adverse event record from the clinical studies and establish causality or confirm the reported causality for all the adverse events.
  • Coordinating for sponsor and Regulatory audits.
  • Perform other related duties as assigned by Head of the department or designee / Line Manager.
  • MBBS pass out can apply for this position.
  • No. of positions - 2


To grow with us, please send your CV to hr@jeevanscientific.com or complete below details.

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