Olema Oncology
Overview
Lead Talent Acquisition Partner at Olema Oncology. Olema Oncology is a cancer medicines company dedicated to impacting breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a differentiated oral medicine known as a complete estrogen receptor antagonist (CERAN) initially in development for metastatic breast cancer. Our pipeline also includes OP-3136, a potent, selective oral inhibitor of the KAT6 pathway. At Olema, we are building a focused team committed to our mission with intention and clarity. Working alongside a talented passionate group of leaders and advisors, we strive to create better medicines that aim to help patients feel better, longer. For more information, visit us at www.olema.com. Role: Associate Director, Clinical Science. As the Associate Director, Clinical Science reporting to the Director, Clinical Science, you will play a key role in one of our ongoing clinical studies. You will collaborate within a multi-disciplinary team—including Clinical Operations, Medical Monitors, Data Management, Biostatistics, Clinical Pharmacology, Regulatory, and Program Management—to plan, conduct, and analyze clinical trials. Your work contributes to Olema’s mission of developing therapies that offer the potential to improve outcomes for women living with cancer. This role may be based out of our San Francisco, CA or Cambridge, MA office and will require up to 15% travel. Primary focus: planning, conducting, and analyzing clinical trials in collaboration with cross-functional teams. Responsibilities
Assist in writing clinical documents including protocols, amendments, investigator’s brochures, clinical study reports (CSR), and the clinical sections of regulatory documents. Interact with investigators and thought leaders in oncology to facilitate the design of clinical synopsis and protocols. Participate in ongoing clinical data review in collaboration with a cross-functional team. Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and subject safety. Contribute to writing and/or review of abstracts, publications, and support the development of presentations for scientific meetings. Additional responsibilities: Collaborate with Clinical Operations and other internal study teams to develop Informed Consent Forms, Case Report Forms, and CRF instructions. Collaborate with Clinical Operations and other team members to develop agendas, training materials, and presentations for site visits, investigator meetings, and other study-related activities. Ensure adherence to Olema’s Standard Operating Procedures and values, maintaining high ethical standards by leading by example. Maintain clinical and technical expertise in the therapeutic area of oncology. Attend scientific meetings pertinent to clinical science activities. Ideal Candidate Profile
Self-Motivated Clinical Scientist. A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees play a unique and crucial role in our success. We are looking for someone with the right combination of knowledge, experience, and attributes for this role. Knowledge: Advanced degree such as a PhD or PharmD; equivalent combination of relevant education and experience may also be considered. Experience in oncology clinical development is required. Ability to interact effectively within a cross-functional team. Experience: 5-7+ years’ experience working as a clinical scientist in the biotech/pharmaceutical industry. Comprehensive knowledge of oncology clinical trial implementation and drug development process. Demonstrated understanding of the clinical drug development process to execute drug development strategic plans and meet milestones. Strong knowledge of Good Clinical Practices (GCP), FDA, and EMEA/CHMP regulations and guidelines; familiarity with other international regulatory requirements is a plus. Ability to proactively identify challenges/problems and propose solutions with a strong sense of urgency. Demonstrated success motivating internal and external team members and collaborators, fostering teamwork. Attributes: Strong attention to detail. Excellent written and oral communication skills. Ability to work in a diverse and dynamic cross-functional team. Passionate about the drug-development process. Self-starter who thrives in a fast-paced environment. The base pay range for this position is expected to be $200,000 - $215,000 annually; however, the base pay offered may vary depending on location, market, job-related knowledge, skills and capabilities, and experience. The total compensation package includes equity, bonus, and benefits. Important Information
We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated. We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants. Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you. Fraud Alert:
We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.
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Lead Talent Acquisition Partner at Olema Oncology. Olema Oncology is a cancer medicines company dedicated to impacting breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a differentiated oral medicine known as a complete estrogen receptor antagonist (CERAN) initially in development for metastatic breast cancer. Our pipeline also includes OP-3136, a potent, selective oral inhibitor of the KAT6 pathway. At Olema, we are building a focused team committed to our mission with intention and clarity. Working alongside a talented passionate group of leaders and advisors, we strive to create better medicines that aim to help patients feel better, longer. For more information, visit us at www.olema.com. Role: Associate Director, Clinical Science. As the Associate Director, Clinical Science reporting to the Director, Clinical Science, you will play a key role in one of our ongoing clinical studies. You will collaborate within a multi-disciplinary team—including Clinical Operations, Medical Monitors, Data Management, Biostatistics, Clinical Pharmacology, Regulatory, and Program Management—to plan, conduct, and analyze clinical trials. Your work contributes to Olema’s mission of developing therapies that offer the potential to improve outcomes for women living with cancer. This role may be based out of our San Francisco, CA or Cambridge, MA office and will require up to 15% travel. Primary focus: planning, conducting, and analyzing clinical trials in collaboration with cross-functional teams. Responsibilities
Assist in writing clinical documents including protocols, amendments, investigator’s brochures, clinical study reports (CSR), and the clinical sections of regulatory documents. Interact with investigators and thought leaders in oncology to facilitate the design of clinical synopsis and protocols. Participate in ongoing clinical data review in collaboration with a cross-functional team. Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and subject safety. Contribute to writing and/or review of abstracts, publications, and support the development of presentations for scientific meetings. Additional responsibilities: Collaborate with Clinical Operations and other internal study teams to develop Informed Consent Forms, Case Report Forms, and CRF instructions. Collaborate with Clinical Operations and other team members to develop agendas, training materials, and presentations for site visits, investigator meetings, and other study-related activities. Ensure adherence to Olema’s Standard Operating Procedures and values, maintaining high ethical standards by leading by example. Maintain clinical and technical expertise in the therapeutic area of oncology. Attend scientific meetings pertinent to clinical science activities. Ideal Candidate Profile
Self-Motivated Clinical Scientist. A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees play a unique and crucial role in our success. We are looking for someone with the right combination of knowledge, experience, and attributes for this role. Knowledge: Advanced degree such as a PhD or PharmD; equivalent combination of relevant education and experience may also be considered. Experience in oncology clinical development is required. Ability to interact effectively within a cross-functional team. Experience: 5-7+ years’ experience working as a clinical scientist in the biotech/pharmaceutical industry. Comprehensive knowledge of oncology clinical trial implementation and drug development process. Demonstrated understanding of the clinical drug development process to execute drug development strategic plans and meet milestones. Strong knowledge of Good Clinical Practices (GCP), FDA, and EMEA/CHMP regulations and guidelines; familiarity with other international regulatory requirements is a plus. Ability to proactively identify challenges/problems and propose solutions with a strong sense of urgency. Demonstrated success motivating internal and external team members and collaborators, fostering teamwork. Attributes: Strong attention to detail. Excellent written and oral communication skills. Ability to work in a diverse and dynamic cross-functional team. Passionate about the drug-development process. Self-starter who thrives in a fast-paced environment. The base pay range for this position is expected to be $200,000 - $215,000 annually; however, the base pay offered may vary depending on location, market, job-related knowledge, skills and capabilities, and experience. The total compensation package includes equity, bonus, and benefits. Important Information
We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated. We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants. Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you. Fraud Alert:
We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.
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