What are the responsibilities and job description for the Clinical Trial Manager position at Ocugen?
Job Details
Job Location
Main Corporate Office - Malvern, PA
Description
Job purpose
The Clinical Trial Manager drives and oversees the operational execution of clinical studies. This individual is responsible for the delivery of clinical studies according to agreed cost and timelines while ensuring patient safety and data integrity and quality.
Duties And Responsibilities
This position operates in an office setting and may include 20% of travel to visit sites, vendors or CROs if needed. Job may require incumbent to be available outside of these hours to handle priority business needs.
Physical Requirements
This is a largely sedentary role.
Ocugen is an equal opportunity employer. In order to provide equal employment and advancement opportunities to all individuals, we make all of our employment decisions based upon merit, qualifications, abilities, and an individual’s conduct and performance. We will not make any of our decisions, and will not discriminate against any employee or applicant, on the basis of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including sexual orientation, gender identity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past, current or prospective service in the uniformed services, genetic information, or any other characteristic protected from discrimination under the law. Ocugen complies with applicable federal, state and local laws governing nondiscrimination in employment.
Job Location
Main Corporate Office - Malvern, PA
Description
Job purpose
The Clinical Trial Manager drives and oversees the operational execution of clinical studies. This individual is responsible for the delivery of clinical studies according to agreed cost and timelines while ensuring patient safety and data integrity and quality.
Duties And Responsibilities
- Develops and directs clinical study and operational activities and manages their execution to ensure completion according to project timelines and budget.
- Leads the study execution team ensuring that studies are conducted in adherence to study protocols, applicable SOPs, ICH/GCP guidelines and government regulations.
- Reviews and contributes to development of protocols, amendments, case report forms and clinical study reports. Develops informed consents and may contribute to development of annual reports and investigational brochures.
- Drives the identification, assessment, and qualification of clinical research sites. Ensures training of all investigational sites including planning of Investigator Meetings and development of stie training materials.
- Drives the new clinical site startup activities.
- Develops study operational documents which may include timelines, enrollment projections and study plans. Tracks performance relative to timelines and projections and ensures compliance with study plans.
- Works collaboratively with internal CRAs to ensure oversight of site initiation, interim monitoring, and site closure activities. Ensures the TMF is developed, maintained, reconciled, and archived.
- Assists in the identification and selection of clinical vendors. May manage the RFI and RFP process.
- Manages clinical vendors tracking of deliverables to ensure they are within timeline and budget.
- Provides study status updates to senior management and escalates study risks, as applicable.
- Works collaboratively with colleagues in Quality Assurance to develop and administer a study audit plan.
- Works collaboratively with colleagues in Finance to forecast, phase and manage study budgets.
- Ensures timely delivery of data for external safety board reviews as applicable.
- Proactively identifies risks, developing and implementing mitigation plans as applicable.
- May manage CROs if needed, and track clinical trial activities.
- May assist in developing policies and procedures (SOPs).
- Additional tasks and projects as requested.
- BA/BS degree, in life sciences.
- 5 years of progressive clinical research experience in the biotechnology/pharmaceutical industry with a 2 years of experience as a Clinical Trial Manager.
- Must have vendor management experience.
- Experience in Ophthalmology and/or advanced therapy studies in Phases 1-3 highly desired.
- Strong knowledge of GCPs, ICH, and FDA regulatory requirements governing human clinical studies.
- Demonstrated attention to detail and outstanding organization skills.
- Self-motivated with a commitment to high quality, on-time deliverables.
- Excellent communication and collaboration skills with a team-oriented approach.
- Experience with eTMF, CTMS and EDC.
- Demonstrated ability to identify and resolve issues and effectively manage timelines.
This position operates in an office setting and may include 20% of travel to visit sites, vendors or CROs if needed. Job may require incumbent to be available outside of these hours to handle priority business needs.
Physical Requirements
This is a largely sedentary role.
Ocugen is an equal opportunity employer. In order to provide equal employment and advancement opportunities to all individuals, we make all of our employment decisions based upon merit, qualifications, abilities, and an individual’s conduct and performance. We will not make any of our decisions, and will not discriminate against any employee or applicant, on the basis of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including sexual orientation, gender identity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past, current or prospective service in the uniformed services, genetic information, or any other characteristic protected from discrimination under the law. Ocugen complies with applicable federal, state and local laws governing nondiscrimination in employment.
