5 - 10 years
5 - 15 Lacs
Posted:1 week ago|
Platform:
Work from Office
Full Time
We are seeking a proactive and results-driven **Business Development Manager** to independently drive lead generation and conversion across domestic and international markets. The ideal candidate should have strong networking skills within the **CRO industry**, and proven experience in securing business from **Pharma, Agrochemicals, Industrial Chemicals, Vaccines, Generics, and Medical Devices** clients.
This role requires working knowledge of **GLP compliance**, **regulatory affairs**, **toxicology studies**, and familiarity with submission processes to global regulatory bodies.
* Independently generate, qualify, and convert leads for preclinical research services.
* Submit tailored technical and commercial quotations to potential clients.
* Network extensively across Pharma, Agrochemical, Vaccine, Generic Drug, Medical Device, and Chemical industries.
* Understand client requirements and align them with organizational capabilities in **GLP and non-GLP studies**.
* Develop and maintain strong client relationships to drive repeat and long-term business.
* Coordinate with internal scientific and operational teams to design study proposals and timelines.
* Provide market intelligence and competitor analysis to support strategic planning.
* Track, monitor, and support **regulatory submissions** to international authorities such as USFDA, EMA, WHO, PMDA, ANVISA, etc.
* Stay updated with global guidelines relevant to **Mammalian Toxicology**, **Ecotoxicology**, and **Regulatory Submissions**.
* Promote services across **small and large animal studies**, including rodent, canine, minipig, and non-human primate models.
* Collaborate on proposals for government and international grants or tenders (if applicable).
* Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields.
* Minimum 2–15 years of BD experience in a CRO or related preclinical research setting.
* Strong understanding of **GLP requirements** and study types.
* Working knowledge of **toxicology, pharmacology, ecotoxicology**, and **regulatory pathways**.
* Familiarity with **GTC (General Toxicity Category)** studies and their scope.
* Excellent communication, negotiation, and relationship-building skills.
* Self-motivated and target-oriented with strong business acumen.
* Willingness to travel domestically and internationally as required.
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* Exposure to **OECD, ICH, USFDA, EPA, REACH, and other regulatory guidelines**.
* Experience in handling **multi-national clients** and long-term contracts.
Survey # 349/A,
Pregnapur Village, Gajwel Mandal.
Siddipet District, PIN 502311,Telangana, India.
Regards,
Chandra Kanth | HRD
Virinchi Technologies
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