o2h group hiring Group Leader, Ph.D. in Pharma Apply

o2h group seeds new ideas in science, technology and green innovation. We work across boundaries and take a collaborative and shared approach to innovation, and therefore we co-invest, co-create and co-execute to bring these ideas to life. o2h group is organised into 6 symbiotic verticals; o2h ventures, o2h discovery, o2h therapeutics, o2h technology, o2h co-work, and o2h community.

Post : Group Leader - In-Vitro ADME and In-Vivo PK Studies

Job Description
Seeking an experienced and motivated Group Leader to oversee our In-Vitro ADME (Absorption, Distribution, Metabolism, and Excretion) and in-vitro PK (Pharmacokinetics) studies. This role is pivotal in our drug development efforts, as it involves managing both in-house in-vitro ADME studies and collaborating with external partners, such as Contract Research Organizations (CROs), for in-vivo PK studies.

Key Responsibilities
• Leadership : Lead and mentor a team of scientists and researchers engaged in in-vitro ADME studies. Provide guidance, set performance expectations, and foster a collaborative and innovative work environment.
• In-Vitro ADME Studies : Oversee the design, execution, and interpretation of in-vitro ADME experiments, including drug metabolism, transport, and drug-drug interaction studies.
• Collaboration with CROs: Establish and maintain relationships with partner CROs for in-vivo PK studies. Coordinate the planning, execution, and monitoring of in-vivo PK studies conducted externally.
• Study Design : Contribute to the design and optimization of in-vitro ADME and in-vivo PK experiments to support drug development projects. Ensure studies are conducted in compliance with regulatory guidelines.
• Data Analysis : Analyze and interpret study data, prepare reports, and present findings to internal teams and external stakeholders.
• Budget Management : Manage the budget for in-vitro ADME studies and collaborate with finance teams to ensure cost-effective execution of in-vivo PK studies conducted at CROs.
• Continuous Improvement : Drive process improvements, implement best practices, and explore new technologies and methodologies to enhance the efficiency and quality of ADME and PK studies.
• Cross-Functional Collaboration : Collaborate closely with other research and development teams to ensure seamless integration of ADME and PK data into drug development projects.
• Client Communication :
* Act as the primary point of contact for clients regarding in-vitro ADME and in-vivo PK studies, ensuring clear and effective communication throughout the project lifecycle.
* Collaborate closely with clients to understand their specific needs, expectations, and timelines.
* Address client inquiries, provide regular progress updates, and manage client feedback and expectations.
• Terms and Conditions (TCs) :
* Review and negotiate project-specific terms and conditions with clients, ensuring alignment with the organization's policies and capabilities.
* Collaborate with BD/BD-Ops teams to finalize and execute contracts and agreements.
• Monthly MIS (Management Information System) Reporting:
* Prepare and deliver monthly updates and reports to senior management, summarizing project progress, key milestones, resource allocation, and any potential challenges or deviations from the project plan.
* Provide insights and recommendations to senior management for informed decision-making and strategic planning.
* Ensure that MIS reports are accurate, comprehensive, and aligned with organizational goals.

Candidate Profile
• Ph.D. in Pharmaceutical Sciences, Pharmacology, or a related field.
• Minimum of 8 years of experience in in-vitro ADME and in-vivo PK studies within the pharmaceutical or biotechnology industry.
• Strong leadership and team management skills.
• Proficiency in designing and conducting in-vitro ADME experiments
• Experience in managing relationships with CROs and overseeing in-vivo PK studies conducted externally.
• Excellent analytical and problem-solving abilities.
• Knowledge of regulatory requirements and compliance in ADME and PK studies.
• Effective communication and presentation skills.
• Detail-oriented and results-driven.
• Ability to work collaboratively in a multidisciplinary environment.
• Excellent interpersonal and client-facing communication skills.
• Experience in contract negotiation and management.
• Proficiency in using MIS tools and software for data analysis and reporting.
• Ability to distill complex technical information into concise and understandable updates for senior management.
• Strong project management skills, including the ability to prioritize tasks, manage multiple projects simultaneously, and meet deadlines.
• Commitment to maintaining client confidentiality and upholding the highest ethical standards in all interactions.

Additional Information
Experience : 8 years
Qualification : Ph.D. in Pharmaceutical Sciences, Pharmacology
Location : Ahmedabad, Gujarat
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : In-Vitro ADME and In-Vivo PK Studies
End Date : 30th January, 2024