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Job Listings - India

With SIRO en route a fresh round of expansion in the New Year 2017, we are looking for bright young sparks to join our burgeoning team! If you have it in you, send across your CV to careers@siroclinpharm.com today! Please mention the title and code for which you wish to apply in the subject line.

We are looking for talented, enthusiastic clinical research professionals for the following positions:

Position Job Code Experience No. of Vacancies
Assistant Manager - Publication Writing MW01 Profile: Publication writing & reviewing experience. Authored Publications in Indexed journals. Conversant with AMA, CONSORT, ICMJE and other publication Guidelines. Copy-Editing skills.

Qualification: BAMS, BHMS, BDS), MD/MS, Ph.D. and/ or post graduate in Pharmacy or life sciences. CMPP Certified desired.

Experience: 5 to 7 years relevant experience for Medical graduates/ & Ph.Ds. More than 7 years relevant experience for post graduates in Pharmacy or life sciences. Oncology & HEOR experience desirable.
1
Biostatistician MW02 Profile: Statistical analysis of Clinical trial (Phase I-IV) data; generation of SAP for Phase II & III studies, Estimation of sample Sizen, Inputs to study protocol & CSR, Generation of randomization schedule and also efficacy datasets, Create and validate tables and listings, Creation of Statistical Analysis Report.

Qualification: Masters in Statistics.

Experience: Statistical analysis experience of a minimum of 4 years.
1
Senior/Principal Regulatory Medical Writer MW03 Profile: Draft CSRs, IB Updates, Protocols, and Narratives. Perform review of CSRs, IB Updates and Protocols. QC CSRs, IB, Protocols, OHA documents and TOS. CTRR experience would be an added advantage.

Qualification: Graduate in Medical Sciences or Post Graduate in Life Sciences, Medical, Dental or Allied Medical Sciences.

Experience: Minimum 4 years in Regulatory Medical Writing with specific experience in CSRs, IB, protocol, narratives.
1
HEOR Analyst MW04 Profile: HEOR Publication writing experience. Authored Publications. Prepare HEOR/ RWE manuscripts/ research papers, review articles, abstracts, posters, slide sets/ oral presentations and other HEOR deliverables like literature review/ analysis, HEOR analysis/ meta-analysis etc. Completely accountable and responsible for assigned activities like writing, review, literature search, project management and leading the project. Good command over English and well conversant with AMA, CONSORT, ICMJE and other HEOR publication guidelines. Meta-analysis/ network analysis hands-on exposure.

Qualification: Qualified doctor (MBBS, BAMS, BHMS, BDS), MD/MS, Ph.D. and/ or post graduate in Pharmacy or life sciences. CMPP certified desired.

Experience: 1 to 2 years relevant HEOR experience for medical graduates/ Ph.Ds; more than 3 years relevant experience for post graduates in Pharmacy or life sciences.
1
Assistant Project Manager MW05 Profile: Project management for assigned clinical trials. Create and implement project management plans, provide updates to sponsor, lead sponsor and internal study meetings. Tracking study progress, achievements of milestones and project finance. Perform interim quality review of study TMF’s. Review of site visit reports and site performance. Lead and mentor CRA, review their performance. Act as clinical lead under Project Manager/Sr. Project Manager for major/important trials. May be required to back-up CRA in case of urgent site visits. Willingness to travel for 15-16 days of month to multiple locations in India.

Qualification: Post Graduate in Chemistry. Basically from Science background.

Experience: Minimum 6 to 7 years of experience in Onsite Monitoring including 1 to 2 years of team lead experience.
1
SAS/ Senior SAS Programmer MW06 Profile: Create and/or validate SAS programs of tables, figures and listings (TFL) for safety and efficacy outputs in required format as per specifications. Annotation of CRF, creation of mapping/ specification documents, programming and/or validation of SDTM, ADaM datasets and define .xml in line with the implementation on CDISC standards.

Qualification: Graduate/ Post Graduate in Life Sciences/ Information Technology/ Statistics/ Engineering.

Experience: SAS Programming experience of a minimum of 2 years.
1
Clinical Research Associate/ Sr. Clinical Research Associate MW07 Profile: Perform site feasibility, site selection visit as per protocol and sponsor requirement. Perform site initiation visit to train study personal on protocol, regulatory and sponsor requirements. Perform routine monitoring at sites which would include source data verification, IP accountability, lab data review etc. Willingness to travel for 15-16 days of month to multiple locations in India.

Qualification: Post Graduate in Chemistry. Basically from Science background.

Experience: Minimum of 2 years for CRA & 4 years for Sr. CRA of experience in Onsite Monitoring of Clinical Trial Sites.
1
DSRM Reviewer MW08 Profile: DSRM writing & reviewing experience (PSUR/ DSUR). RMP & REMS authoring & QC experience; DSUR/ SUSAR coordination; RMP writing/ QC; Lay summary exposure. Well conversant with E2F and E2E/ E2R & other PV guidelines.

Qualification: Qualified doctor (MBBS, BAMS, BHMS, BDS), MD/MS, Ph.D. and/ or post graduate in Pharmacy or life sciences. Pharmacovigilance experience desired.

Experience: 3 to 4 years relevant experience for medical graduates, masters in life sciences/ more than 5 years relevant experience for science graduates. RMP/ REMS experience.
2
Publication Writer/ Reviewer MW09 Profile: Publication writing & Reviwing experience. Good command over English and well conversant with AMA, CONSORT, ICMJE and other publication guidelines. Authored Publications in Indexed journals. Copy-Editing skills. Should be able to understand and communicate with authors/approvers/KOLs to address specific comments, modifications etc. in the publications.

Qualification: Qualified doctor (MBBS, BAMS, BHMS, BDS), MD/MS, Ph.D. and/ or post graduate in Pharmacy or life sciences. CMPP Certified preferred.

Experience: 3 to 4 years relevant experience for medical graduates/ Ph.Ds; more than 5 years relevant experience for post graduates in Pharmacy or life sciences. Oncology & HEOR experience.
4
Sr. Publication Writer/ Principal Publication Writer MW11 Profile: Authored Publications in Indexed journals. Prepare and review manuscript/ research papers, review articles, abstracts, posters, slide sets/ oral presentations. Be completely accountable and responsible for assigned activities like writing, review, literature search, project management and leading the project. Good command over English and well conversant with AMA, CONSORT, ICMJE and other publication guidelines. Copy-Editing skills.

Qualification: Qualified doctor (MBBS, BAMS, BHMS, BDS), MD/MS, Ph.D. and/ or post graduate in Pharmacy or life sciences. CMPP Certified preferred.

Experience: 3 to 4 years relevant experience for medical graduates/ Ph.Ds; more than 5 years relevant experience for post graduates in Pharmacy or life sciences. Oncology & HEOR experience desired.
4
Sr. HEOR Analyst MW12 Profile: Prepare and review HEOR/ RWE manuscripts/ research papers, review articles, abstracts, posters, slide sets/ oral presentations and other HEOR deliverables like literature review/ analysis, HEOR analysis/ meta-analysis etc. Be completely accountable and responsible for assigned activities like writing, review, literature search, project management and leading the project. HEOR Publication writing & Reviewing experience. Authored Publications. Well conversant with AMA, CONSORT, ICMJE and other HEOR publication guidelines. Copy-Editing; meta-analysis/ network analysis hands-on exposure.

Qualification: Qualified doctor (MBBS, BAMS, BHMS, BDS), MD/MS, Ph.D. and/ or post graduate in Pharmacy or life sciences. CMPP Certified.

Experience: 3 to 4 years relevant HEOR experience for medical graduates/ Ph.Ds; more than 5 years relevant experience for post graduates in Pharmacy or life sciences. Meta-analysis/ network analysis hands-on exposure.
1