Delivering the best services is accomplished by hiring the best. Our team stand as pillars that hold up every quality promise that we make. That’s why, we at Bio Scientific Research Laboratories (I) Pvt Ltd are always looking for qualified and energetic individuals, with a desire for excellence, to join our team.
We provide an environment that gives people the chance to achieve their goals, both professionally and personally. At Bio Scientific Research Laboratories (I) Pvt Ltd, we offer you various opportunities to develop yourself, room to explore your talent and offer attractive remuneration with benefits which form a stepping stone to building your career.
Current Openings:
Please share your CV at hr@biosrl.com so that we can contact you once the suitable openings are available.
Sr. Analyst
Hiring for Sr. Analyst. Interested candidates can send their CVS on hr@biosrl.com and contact on 8879502044.
No. of vacancies: 03
Experience: Minimum 3 years of BA/BE CRO
Qualification: M. Pharm./M.Sc.
- Capable to perform routine work on instrument's AB Sciex LC-MS/MS.
- To monitor and give a first check for the activities completed by Analyst, Jr. Analyst and Trainees.
- Preparation and compilation of the Method Development Report, Method Validation protocol and Standard Testing Procedure and reports of respective validation and projects. 4) Capable to perform routine activity in Bioanalytical Lab.
- Perform Method development, Method validation and Subject sample analysis as per GDP and in house SOPs.
- Preparation of Stock solution, Spiking solution and Biological Samples.
- Knowledge of Method Validation and subject sample analysis of regulatory norms.
- Compilation of Raw data for Method validation and Subject sample analysis, logbooks, Calibration documents and other lab related documents submission to QA for archival.
Sr. CRA (Medical writer)
Hiring for Sr. CRA (Medical writer). Interested candidates can send their CVS on hr@biosrl.com and contact on 8879502044.
No. of vacancies: 01
Experience: 3-5 years BAIBE CRO experience
Qualification: B. Pharm, M. Pharm
- Preparation of Protocol, study specific informed consent form and other regulatory documents.
- Preparation of Clinical Study Report after completion of study.
- Preparation and review of clinical SOPs.
- Raise change control documentation for clinical SOP, Instrument and equipment.
- Performing screening related activity like registration, biometric verification, demographic examination, alcohol consumption test, drug of abuse test. 6) Assist the principal investigator in conduction of protocol meeting.
- Distribution of ICF for volunteers and group counselling of subjects.
- Assist the physician/ Principal investigator/ Clinical investigator in presentation of informed consent form.
- Preparation of labels for sample collection and sample storage.
- Conducting and monitoring dispensing and dosing activity.
- Performing sample processing, sample segregation and transfer activity.
- Monitoring clinical activities like blood collection, sample processing, meals and restriction activities.
- Preparation, reviewing and compilation of study documents (TMF, CRF, ICF etc.).
- Recording the subject check in and check out details.
- Coordinate with clinical vendor like canteens, pathology lab, hospital, ambulance services, insurance company for study intimation.
Male Nurse
Hiring for Male Nurse. Interested candidates can send their CVS on hr@biosrl.com and contact on 8879502044.
Experience: Fresher or 1-2 years
Qualification: GNM/ANM
- Pre study preparation of ICU
- Preparation of cannulation trolley
- Vital recording
- Assisting phlebotomy and blood collection
- Study day activities
- Monitoring temperature and humidity in ICU area
- ICU Equipment responsibilities
- Emergency handling in case of AE / SA
- Any other work to perform any other duties as required by company related to Protocol of study. /li>
Physician
Hiring for Physician. Interested candidates can send their CVS on hr@biosrl.com and contact on 8879502044.
- BABE and Phase Trials. ICH-GCP and ethical aspects for conduct of a clinical trial study.
- execution teams to work upon clinical studies across two different clinical study management.
- Providing valuable medical inputs to the Medical Writing team comprising of protocol writers and report writers. Organize and schedule activities from protocol writing, IEC submission and eCTD specification for study report submission
- Manage a volunteer registration and management unit with a volunteer registration data base comprising
- Establish firm execution systems and SOP's governing clinical execution aspects and completed studies with GCP compliance.
- Reporting recording and management of several adverse events in accordance with safety principles and regulatory guidance.
- Establish Adverse Event tracking system which aided in following volunteers who encountered adverse events
- Devise strategies across sample processing area and ensure minimal logistics utilization for cold chain maintenance for samples.
- Establish eCRF documentation for source data management
- Preparation of Patient Information Leaflets
- Scrutinizing healthy volunteers for BA/BE study in coordination with Principal Investigator.
- Supervise day to day activity assigned to study personnel.
- Ensuring the proper functioning of Emergency care equipment’s before study commencement and throughout study period.
- Supervise day to day activity assigned to study personnel.
Clinical QC
Hiring for Clinical QC. Interested candidates can send their CVS on hr@biosrl.com and contact on 8879502044.
Experience: 1-3 Years in Clinical QC in CRO
Qualification: B. Pharma/ M. Pharma/ M. SC
- Review of pre-study file, during study and post study files, vaccutainer/vial labels, log books, completed ICF and CRFs in timely manner.
- Ensuring that all staff involved in the study is trained in protocol.
- Ensure that all the activities are been done as per protocol ,SOP’s and GCP
- Assessing in pharmacy related activities (like Acceptance, labeling, dispensing, reconciliation and storage of IP’s)
- Online monitoring and taking print of the temperature record from the software.
- Providing study related information to the Ethics Committee, Contracted hospitals and Insurance company.
- Preparation of study up-dates after completion of the study and send it to technical Documentation.
- Preparation of Statistical up-date and send it to the respective person.
- Review clinical report