CrawlJobs Logo
Enveda Logo Enveda · Research and Development

Director - ADME

India, Hyderabad · Job Posted January 16, 2026
Apply Position
Job Link Share

Job Description

Join Enveda as an Director, ADME in Hyderabad, India, and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation—are you ready to make a difference? At Enveda, every role drives impact.As Director, ADME, you will build and lead a high-impact ADME function, working closely with Medicinal Chemistry, Pharmacology, and Non-Clinical teams to rapidly advance discovery programs. Reporting to the Chief Development Officer, you’ll influence strategy, execution, and talent development across the drug discovery lifecycle.

Job Responsibility

  • Provide scientific leadership on ADME–SAR, guiding medicinal chemistry to enhance druggability
  • Define and execute DMPK strategies across early discovery and lead optimization
  • Lead in vitro and in vivo ADME study design, execution, and interpretation
  • Oversee bioanalytical method development, validation, and qualification
  • Analyze, interpret, and communicate ADME/DMPK data to internal and external stakeholders
  • Partner with Non-Clinical teams on PK/PD study design and candidate selection
  • Build, mentor, and lead a high-performing ADME organization, including SOP and capability development
  • Ensure compliance with data integrity, safety, quality, and audit requirements
  • Direct ADME lab operations, including CAPEX/OPEX planning, resource optimization, and instrument management
  • Deliver clear project and departmental updates to senior leadership

Requirements

  • PhD in Pharmaceutical Sciences or a related discipline
  • 15+ years of post-PhD experience in ADME/DMPK within drug discovery or development
  • Proven experience setting up and leading ADME functions
  • Strong understanding of regulatory, safety, and audit requirements
  • A collaborative leader who enjoys mentoring, building teams, and working cross-functionally

What we offer

  • Culture
  • Medical
  • Block Leaves
  • Work-Life Harmony
Enveda - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Director - ADME

8 matching positions

Director, Clinical Pharmacology

The role is positioned in the Clinical Pharmacology group, Clinical and Quantita...
Location
Location
United States , Cambridge
Salary
Salary:
167000.00 - 300700.00 USD / Year
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD and/or PharmD in Clinical Pharmacology, Pharmacometrics, Pharmaceutics, Statistics, Engineering, or a related field with a minimum of 8-10 years of industry experience in clinical pharmacology
  • In depth knowledge of clinical pharmacology, PK/PD principles, modeling and simulation, ADME and quantitative translational sciences
  • Hands-on quantitative skills, modeling expertise and familiarity with clinical operations and translational sciences
  • Sound knowledge of drug regulatory authority biopharmaceutics and clinical pharmacology requirements to support the clinical development and marketing of new drug products
  • Drug development experience in oncology and rare diseases preferred
  • expertise in immune therapeutics and/or infectious diseases is a plus
  • Platform expertise in mRNA therapeutics, and/or experience with biologics and new modalities preferred
  • Demonstrated ability to work independently, lead functional initiatives, adapt quickly and collaborate effectively in a highly dynamic environment and influence cross-functional teams
  • Proficient in using pharmacokinetic, modeling and data visualization software (e.g. Phoenix WinNonlin, R, Monolix, NONMEM, etc)
  • Outstanding verbal and written communication skills, with the ability to distill complex data for diverse audiences
Job Responsibility
Job Responsibility
  • Develop a fit-for-purpose Clinical Pharmacology development plan, including dose selection and optimization, evaluation plan for special populations, PK/PD and immunogenicity assessment, and pediatric development
  • Collaborate with program teams to develop dose selection strategy and support decision makings for first-in-human studies and IND submissions
  • Represent CQP in a highly matrixed team setting to drive study execution and operational excellence toward product development goals
  • Lead the development of CQP related sections in regulatory documents (e.g., clinical protocols, INDs, regulatory meeting briefing books, summary documents for BLAs, responses to regulatory authorities) and represent clinical pharmacology in regulatory interactions
  • Lead/oversee the Clin Pharm data analysis, interpretation, and reporting to inform clinical implications and development decisions
  • Advocate and represent clinical pharmacology and MIDD strategies with internal and external stakeholders
  • Mentor junior team members to contribute to the development of a high-performing Clinical Pharmacology team
  • Leverage literature data and collaborate with external consultants, CRO partners and academic sites to problem solve and develop solutions to clinical pharmacology issues and grow organizational knowledge on mRNA platform
What we offer
What we offer
  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities to help you plan for the future
  • Location-specific perks and extras
  • Annual discretionary bonus, other incentive compensation, or equity award
  • Fulltime
Read More
Arrow Right

Director of Agency Development

Orchid Insurance, an Arrowhead Intermediaries company, is seeking a Director of ...
Location
Location
United States , Tampa
Salary
Salary:
Not provided
bbrown.com Logo
Brown & Brown UK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 7 plus years P&C industry experience
  • Minimum of 5 plus years of experience in account management, agency development, outside sales experience, or similar role
  • Demonstrates strong leadership qualities such as the ability to inspire and motivate others, effective decision-making, and a proactive approach to problem-solving
  • Passion to remove obstacles and get the job done
  • Possess a professional demeanor in a fast-paced production environment
  • Be willing to always represent the company with the utmost professionalism
  • Must be team-oriented and able to meet team deadlines
  • Must be results-oriented and thrive in high volume environments
  • Proficiency in MS Office Suite and CRM software such as Salesforce
  • Positive attitude and friendly demeanor
Job Responsibility
Job Responsibility
  • Under the direction of Distribution Management, responsible for the performance of the agency development team and is expected to achieve results through consistent recruitment, training, and supervising activities
  • Ensure proper staffing goals are met, and manage activities associated with the selection and performance of new agency development managers
  • Support the training and education of products across the team, including Personal Lines E&S and Digital partnerships
  • Support ADMs in managing territory operation and implementing action plans to meet or exceed goals and objectives
  • Generate new premium growth through coaching interactions with ADMs (calls, emails, f2f visits, etc.)
  • Cultivate relationships with new and existing assigned agents to direct qualified risk selection
  • Implement proactive efforts including activities that keep agents informed on systems, products, and underwriting guidelines as well as prospecting new agencies and general account management
  • Provide general account management for agencies and maintain accurate records of all sales activities via Salesforce – enforce usage of Salesforce by ADMs
  • Proactively monitor key performance indicators outlier, shares best practices and be solutions oriented
  • Monitor and report newly appointed agency metrics such as quote volume and written premium
What we offer
What we offer
  • Health Benefits: Medical/Rx, Dental, Vision, Life Insurance, Disability Insurance
  • Financial Benefits: ESPP
  • 401k
  • Student Loan Assistance
  • Tuition Reimbursement
  • Mental Health & Wellness: Free Mental Health & Enhanced Advocacy Services
  • Beyond Benefits: Paid Time Off, Holidays, Preferred Partner Discounts and more
  • Fulltime
Read More
Arrow Right

Citrix Expert Consultant

Inetum is looking for a skilled Citrix Expert Consultant to join our team and su...
Location
Location
Portugal , Lisbon
Salary
Salary:
Not provided
https://www.inetum.com Logo
Inetum
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 5 years' experience in a similar Citrix-focused role
  • Solid expertise in Citrix CVAD, NetScaler (Citrix ADC), Citrix ADM, and Citrix Workspace Environment Management
  • Hands-on experience with ControlUp for dashboard management, analysis and automation
  • Strong knowledge of networking concepts (DNS, DHCP, load balancing, SSL VPNs)
  • Proficient in PowerShell scripting
  • Ability to diagnose and resolve complex technical issues
  • Excellent communication and collaboration skills
  • Fluent in English (B2–C1 level)
Job Responsibility
Job Responsibility
  • Design, deploy and manage Citrix Virtual Apps and Desktops (CVAD) environments across on-prem, hybrid and cloud infrastructures
  • Configure and maintain NetScaler (Citrix ADC) for load balancing, secure remote access, and application delivery
  • Implement advanced features such as TLS VPNs, MFA authentication, and performance tuning
  • Use ControlUp for real-time monitoring, troubleshooting, reporting, and process automation
  • Conduct performance reviews, collect feedback, and implement user experience improvements
  • Monitor Citrix platforms using tools such as Citrix Director and ControlUp Insight
  • Document processes and configurations to ensure consistent service quality
  • Collaborate closely with Infrastructure teams (Network, Wintel, Security) and business stakeholders
  • Provide technical support, training and guidance to users and internal IT teams
  • Ensure compliance with internal and external security standards and best practices
  • Fulltime
Read More
Arrow Right

Scientific Associate Director - Pharmacokinetics and Drug Metabolism

In this vital and exciting role, you will oversee Pharmacokinetics and Drug Meta...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD in Pharmacokinetics, Pharmaceutical Sciences, Engineering, or related fields with equivalent professional degrees and 12+ years of experience in the Biotechnology/Pharmaceutical Industry
  • Solid technical experience with the application of SM in vitro/in vivo ADME and pharmacokinetics fundamentals to drug discovery projects
  • Ability to drive the progression of SM discovery and development within project teams
  • Expertise with in vitro ADME, in vivo ADME, PK/PD etc
  • Experience in supporting preclinical components of regulatory documentations
  • Excellent interpersonal, technical, and communication skills
  • Past experience as a laboratory scientist in a pharma or biotech environment
  • Excellent written and oral communication skills, attention to detail and accuracy, and interpersonal skills
  • Record of scientific contributions through peer-reviewed articles and external presentations
Job Responsibility
Job Responsibility
  • Lead/mentor a team of scientists involved in ADME characterization of small molecules
  • Directly responsible for leading a team of scientists involved in undertaking mechanistic in vitro ADME assays
  • Develop/implement novel tools to efficiently support mechanistic ADME work
  • Oversee activities/establish workflows for small molecule bioanalytical and ADME screening teams
  • Serving as a subject matter expert of small molecule ADME to support the programs and recommend strategies to PKDM project team representatives to reduce/mitigate risks due to metabolism
  • Collaborate with scientists across our PKDM scientific community
  • Leveraging specialized ADME/PK skills such as in vitro ADME, in vivo ADME, biotransformation, PK/PD, to impact project progression and decision-making
  • Contributing to the analysis of pre-clinical ADME and PK data for IND and NDA filings and documenting these analyses in appropriate reports
  • Building close relationships with partner functions
Read More
Arrow Right

Director, Medicinal Chemistry

Enveda is looking for a Director, Medicinal Chemistry to join our team in Hydera...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
enveda.com Logo
Enveda
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctor of Philosophy in Synthetic Organic Chemistry
  • 15-20 years of post-PhD experience in Medicinal Chemistry
  • Proven track record of delivery of leads and clinical candidates to the pharmaceutical industry
  • Management and mentoring of synthetic chemists
  • Good understanding of intellectual property of medicinally valuable compounds with respect to composition of matter, method of use and chemical processes
  • Strong understanding of safety practices in organic synthesis laboratories
Job Responsibility
Job Responsibility
  • Lead medicinal chemistry activities for two or more projects in parallel
  • Involved in identifying pre-leads, design and optimization of leads for potency, selectivity and druggability and also strong IP generation
  • Recruit PhD and M. Sc. synthetic chemists and mentor them as medicinal chemists and manage their performance and improve their productivity
  • Collaborate with peers in Medicinal Chemistry and work as a team to increase delivery of compounds to the Clinical Pipeline
  • Collaborate with Senior Leaders in other functional departments such as ADME, Analytical Sciences and Pharmacology and deliver high value molecules
  • Report to the VP, Discovery Chemistry
  • Collaborate on Medicinal Chemistry of Lead Generation and Lead Optimization of Pipeline Projects
  • Understand Structure Activity Relationships and Structure Property Relationships of various projects
  • Collaborate with Medicinal Chemistry, Pharmacology, Analytical, ADME, Tox, IP, Site and Global Leadership
  • Develop appropriate flow schemes with relevant in vitro, in vivo, ADME/PK and tox studies
What we offer
What we offer
  • Culture
  • Medical
  • Block Leaves
  • Work-Life Harmony
  • Fulltime
Read More
Arrow Right
New

Senior Customer Support Service Specialist

At Boeing, we innovate and collaborate to make the world a better place. We’re c...
Location
Location
United States , Hazelwood
Salary
Salary:
104550.00 - 141450.00 USD / Year
boeing.com Logo
Boeing
Expiration Date
July 10, 2026
Flip Icon
Requirements
Requirements
  • 10+ years of experience with F/A-18 and/or EA-18G operations and maintenance
  • 5+ years of experience as a Field Service Representative supporting a Defense System
  • Ability to travel 10% of the time
Job Responsibility
Job Responsibility
  • Provide engineering reach-back technical assistance to Boeing field service representatives located at customer sites worldwide supporting F/A-18 Hornet/Super Hornet and EA-18G Growler aircraft
  • Serve as a Subject Matter Expert (SME) for the following F/A-18 systems: Airframe, Power Plant, Fuel, Hydraulic, Flight Controls, Environmental Control, Secondary Power, Egress
  • Support Boeing modification and production operations
  • Apply advanced engineering techniques and Boeing product support resources to research, develop, analyze and design troubleshooting and repair solutions that comply with customer, regulatory, safety and company requirements
  • Manage the field service VECTOR reporting tool and reviews reports for safety, publications, retrofit, sustainment and engineering impacts
  • Analyze and report metrics
  • Conduct onboarding and technical training for FSRs, as well as aircraft and systems familiarization to customers as requested
  • Publish field service reference materials for FSR and customer use
  • Manage extensive field service reference library and website development
  • Understand customer expectations and operations, coordinates fleet support activities and liaisons with Program Management
What we offer
What we offer
  • Generous company match to your 401(k)
  • Industry-leading tuition assistance program pays your institution directly
  • Fertility, adoption, and surrogacy benefits
  • Up to $10,000 gift match when you support your favorite nonprofit organizations
  • Fulltime
Read More
Arrow Right
New

District Support Pharmacist

We’re building a world of health around every individual — shaping a more connec...
Location
Location
United States , Keene
Salary
Salary:
60.00 - 76.00 USD / Hour
https://www.cvshealth.com/ Logo
CVS Health
Expiration Date
August 25, 2026
Flip Icon
Requirements
Requirements
  • Active Pharmacist License in the state where the Store is located
  • Active National Provider Identifier (NPI)
  • Not on the DEA Excluded Parties list
Job Responsibility
Job Responsibility
  • Living our purpose by helping to manage and improve patient health through safe and appropriate dispensing, counseling, and immunizing practices
  • Traveling the district to fill pharmacist shifts as scheduled by the District Performance Coordinator (DPC)
  • overseeing the pharmacy and serving as the Pharmacy Manager's proxy during bench shifts without overlap
  • Supporting safe and accurate prescription fulfillment by following—and directing the pharmacy team to follow—pharmacy workflow procedures and utilizing the safety guardrails at every workstation
  • Assumes Pharmacy Manager's day-to-day duties when serving as the only or the primary pharmacist-on-duty
  • Contributing to positive patient experiences by showing empathy and genuine care and coaching the pharmacy team to do the same: demonstrating compassionate care, collaborating with the patient's total healthcare team, and proactively resolving insurance and/or medication issues
  • Proactively offering and delivering immunizations to keep patients healthy
  • engaging and supporting Pharmacy Technicians to learn to immunize
  • Supporting the effective management of pharmacy inventory in all pharmacies worked by following—and guiding the pharmacy team to follow—all inventory best practices, with a special focus on protecting cold chain products for our patients and our business
  • Remaining flexible for both scheduling and business needs, while contributing to a safe, inclusive, and engaging team dynamic
What we offer
What we offer
  • medical, dental, and vision coverage
  • paid time off
  • retirement savings options
  • wellness programs
  • other resources
  • Fulltime
Read More
Arrow Right
New

Entry-Level Systems Engineer (Digital Comm & Networks Sys Engrg)

At Boeing, we innovate and collaborate to make the world a better place. We’re c...
Location
Location
United States , El Segundo; Los Angeles
Salary
Salary:
Not provided
boeing.com Logo
Boeing
Expiration Date
July 22, 2026
Flip Icon
Requirements
Requirements
  • This position requires the ability to obtain a US Security Clearance for which the US Government requires US Citizenship as a condition of employment. A final U.S. Secret Clearance Post-Start is required.
  • Bachelor of Science degree from an accredited course of study in engineering, engineering technology (includes manufacturing engineering technology), chemistry, physics, mathematics, data science, or computer science
  • Education or experience in signal processing
Job Responsibility
Job Responsibility
  • Design and develop next generation RF, digital, and optical satellite communication systems
  • Develop and verify multi-rate, fixed-point digitalsignal processing architectures
  • Allocate, define, and verify requirements and interfaces in the development of communication digital payloads
  • Develop performance and link budgets
  • Conduct performance analysis of signal processing models
  • Assist with conducting trade studies
  • Develop prototype demonstrations on flight-like communication subsystem testbeds
  • Support unit-level integration and performance simulations
  • Support ASIC and FPGA level system design and verification
  • Support hardware procurement, design reviews, and unit sell-offs
What we offer
What we offer
  • competitive base pay and variable compensation opportunities
  • health insurance
  • flexible spending accounts
  • health savings accounts
  • retirement savings plans
  • life and disability insurance programs
  • paid and unpaid time away from work
  • generous company match to your 401(k)
  • industry-leading tuition assistance program pays your institution directly
  • fertility, adoption, and surrogacy benefits
Read More
Arrow Right