Codera Jobs Hiring Now
Codera is hiring for 5 open roles on Migrate Mate as of July 16, 2026, concentrated in clinical trials & medical research and procurement & supply chain, with listed salaries up to about $375,000. Migrate Mate updates Codera's live openings daily. Codera is a clinical-stage biotechnology company focused on drug discovery and development, with open positions spanning clinical development, clinical operations, and supply chain leadership.
Find Codera JobsOverview
Codera hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 5
- Top team
- Clinical Trials & Medical Research
- Seniority
- Manager level or above
- Work type
- 0% remote or hybrid
- Top location
- San Diego
- Salary range
- $160,000–$375,000
Listed salaries for Codera roles on Migrate Mate range from about $160,000 to $375,000 per year across 5 open roles, as of July 16, 2026.
Open Roles at Codera
Showing 5 of 5+ Codera jobs
About Codera
Codera is a Tang Capital company that provides in-house end-to-end drug development capabilities for its portfolio companies. Founded in 2002, Tang Capital is a life-sciences focused investment company that creates, acquires and finances companies that develop and commercialize pharmaceutical products.
Position Summary
The Director/Senior Director, Clinical Development will support the clinical development strategy and execution of Codera’s domestic and international drug development programs. Reporting to the Vice President, Clinical Development, this role will contribute to the design, implementation and oversight of clinical trials across all phases of development. The Director/Senior Director, Clinical Development will collaborate cross‑functionally to ensure high‑quality clinical data, support regulatory interactions and provide medical and scientific input throughout the clinical trial lifecycle. This role will also support safety monitoring and pharmacovigilance activities in partnership with internal and external stakeholders.
Essential Duties and Responsibilities
- Support the planning and execution of clinical development programs, ensuring alignment with overall program strategy and timelines
- Contribute to the evaluation and refinement of development strategies to mitigate risks and advance clinical assets efficiently
- Participate in the planning, delivery and cross-functional coordination of clinical trials from early to late phases
- Assist in the development, review and refinement of clinical trial protocols, ensuring scientific rigor, ethical conduct and regulatory compliance
- Provide medical and clinical input throughout the clinical trial lifecycle, including safety monitoring, data interpretation and risk management
- Partner with biometrics and medical writing to ensure clinical and nonclinical studies are designed, analyzed and summarized appropriately in accordance with timelines, good quality practices and applicable regulatory requirements
- Collaborate with regulatory affairs and other departments to support regulatory strategies, clinical trial submissions and responses to health authorities
- Support data analysis and reporting activities, contributing strategic insights to inform decision-making and regulatory submissions
Qualifications
- Bachelor’s Degree required
- Advanced degree preferred
- Minimum 6 years of clinical development experience within the biotechnology or pharmaceutical industry
- Experience with multiple, complex programs or studies
- Detailed understanding of end-to-end management of clinical trial conduct, clinical drug development and clinical trials operations
- Deep understanding of global regulatory requirements and experience navigating clinical trials to approval
- Outstanding written and verbal communication skills, including the ability to use clear language to explain complex ideas
- Possess a willingness and ability to work hands-on in a detail-driven, fast-paced, entrepreneurial environment
- Strategic agility with strong critical and logical thinking and ability to analyze problems
- Ability to establish and maintain collaborative working relationships with internal and external stakeholders
The job description is not designed to cover or contain a comprehensive list of activities, duties or responsibilities that are required. They may change, or new ones may be assigned at any time with or without notice.
The estimated annual base salary for this position is $200,000 - $280,000 commensurate with experience and skills. This role may be eligible for discretionary bonuses and other incentive programs.
Codera provides a comprehensive benefits package designed to support employees’ physical, mental and financial health and include employer sponsored insurance plans including medical, dental and vision coverage; generous paid time off; retirement plan options and additional wellness and professional development programs.
Codera provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Codera participates in E‑Verify. All newly hired employees are required to complete the E‑Verify process as part of their employment eligibility verification.
About Codera
Codera is a Tang Capital company that provides in-house end-to-end drug development capabilities for its portfolio companies. Founded in 2002, Tang Capital is a life-sciences focused investment company that creates, acquires and finances companies that develop and commercialize pharmaceutical products.
Position Summary
The Director/Senior Director, Clinical Development will support the clinical development strategy and execution of Codera’s domestic and international drug development programs. Reporting to the Vice President, Clinical Development, this role will contribute to the design, implementation and oversight of clinical trials across all phases of development. The Director/Senior Director, Clinical Development will collaborate cross‑functionally to ensure high‑quality clinical data, support regulatory interactions and provide medical and scientific input throughout the clinical trial lifecycle. This role will also support safety monitoring and pharmacovigilance activities in partnership with internal and external stakeholders.
Essential Duties and Responsibilities
- Support the planning and execution of clinical development programs, ensuring alignment with overall program strategy and timelines
- Contribute to the evaluation and refinement of development strategies to mitigate risks and advance clinical assets efficiently
- Participate in the planning, delivery and cross-functional coordination of clinical trials from early to late phases
- Assist in the development, review and refinement of clinical trial protocols, ensuring scientific rigor, ethical conduct and regulatory compliance
- Provide medical and clinical input throughout the clinical trial lifecycle, including safety monitoring, data interpretation and risk management
- Partner with biometrics and medical writing to ensure clinical and nonclinical studies are designed, analyzed and summarized appropriately in accordance with timelines, good quality practices and applicable regulatory requirements
- Collaborate with regulatory affairs and other departments to support regulatory strategies, clinical trial submissions and responses to health authorities
- Support data analysis and reporting activities, contributing strategic insights to inform decision-making and regulatory submissions
Qualifications
- Bachelor’s Degree required
- Advanced degree preferred
- Minimum 6 years of clinical development experience within the biotechnology or pharmaceutical industry
- Experience with multiple, complex programs or studies
- Detailed understanding of end-to-end management of clinical trial conduct, clinical drug development and clinical trials operations
- Deep understanding of global regulatory requirements and experience navigating clinical trials to approval
- Outstanding written and verbal communication skills, including the ability to use clear language to explain complex ideas
- Possess a willingness and ability to work hands-on in a detail-driven, fast-paced, entrepreneurial environment
- Strategic agility with strong critical and logical thinking and ability to analyze problems
- Ability to establish and maintain collaborative working relationships with internal and external stakeholders
The job description is not designed to cover or contain a comprehensive list of activities, duties or responsibilities that are required. They may change, or new ones may be assigned at any time with or without notice.
The estimated annual base salary for this position is $200,000 - $280,000 commensurate with experience and skills. This role may be eligible for discretionary bonuses and other incentive programs.
Codera provides a comprehensive benefits package designed to support employees’ physical, mental and financial health and include employer sponsored insurance plans including medical, dental and vision coverage; generous paid time off; retirement plan options and additional wellness and professional development programs.
Codera provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Codera participates in E‑Verify. All newly hired employees are required to complete the E‑Verify process as part of their employment eligibility verification.
Job Roles at Codera
Working at Codera
Codera's 5 open roles are manager level or above, and about 0% are remote or hybrid. The most active teams are clinical trials & medical research and procurement & supply chain. Codera is a clinical-stage biotechnology company working on drug discovery and development programs. Its open positions reflect an organization actively building out clinical development, clinical program management, clinical supply chain, and study start-up functions. Most Codera roles are based in San Diego.
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Browse jobs by roleCodera Jobs: Frequently Asked Questions
How many jobs is Codera hiring for right now?
Codera is hiring for 5 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in clinical trials & medical research and procurement & supply chain. Roles range from associate director to vice president level across clinical development and operations functions. Migrate Mate pulls Codera's latest postings automatically so the count reflects current openings.
What kinds of roles does Codera hire for?
The most active teams are clinical trials & medical research and procurement & supply chain. Codera hires primarily for clinical development, clinical program management, study start-up, and clinical supply chain positions. Additional postings cover director and vice president roles overseeing development strategy. Most postings are manager level or above, reflecting a focus on experienced professionals in clinical operations and drug development leadership.
Are Codera jobs remote or in-person?
Mostly on-site. About 0% of Codera's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in San Diego. Each Codera listing shows its work location so you can filter before applying.
How do I apply to a job at Codera?
Find a Codera role on Migrate Mate, then follow the listing through to Codera's own careers page to complete the application. Codera manages its own hiring process, including resume review, interviews, and offers. Migrate Mate does not collect applications on Codera's behalf.
What do Codera jobs pay?
Listed salaries for Codera roles on Migrate Mate range from about $160,000 to $375,000 per year as of July 16, 2026, with most postings at manager level or above. Exact pay is set by Codera and shown on each listing.
Does Codera hire entry-level?
Most of Codera's open roles on Migrate Mate are manager level or above as of July 16, 2026. Entry-level openings are limited. Check individual Codera listings for stated experience requirements.
Where is Codera hiring?
Most Codera roles are based in San Diego, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.