Smithers

Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development. PDS works with customers to develop new methods, validate existing methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials currently in different phases of the FDA regulated drug approval process. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories.

Smithers PDS is seeking an Associate Project Manager who will be responsible for being the client's primary point of contact and for the overall conduct of the study. The Associate Project Manager ensures deliverables are met on-time, within scope, and within established quality standards.

This position is salaried and is classified as an exempt position. Exempt employees typically work 40 hours or more to adequately perform their responsibilities. Extended work hours may be necessary to support the business in meeting client deliverable commitments. Position is generally eligible for a hybrid work schedule with at least three days on-site once all training requirements have been adequately met and proficient performance is consistently demonstrated.

Salary range for this position is $87,500 - $112,5000 per year. Salary and job title will be commensurate with experience and qualifications. Smithers PDS offers a comprehensive health insurance package including a choice of 3 medical plans, dental insurance, vision insurance, 401K retirement plan and PTO.

Essential Position Responsibilities:

• Responsible for client interaction and the conduct of studies.
• Serve as Principal Investigator for GLP studies
• Responsible for data interpretation, analysis, and reporting of results for validation and sample analysis of biopharmaceutical products.
• Support business development activities.
• Provide technical advice to scientific staff.
• Experience and knowledge of Ligand-binding assays (ELISA / MSD) applicable to Pharmacokinetic, Biomarker and Immunogenicity studies is required.
• Must understand contract immunoanalytical business objectives and is expected to be familiar with regulatory, and GLP requirements, FDA guidelines and industry standards for bioanalytical method validation.
• Knowledge of Watson LIMS a plus.
• Additional responsibilities include forecast of revenue, preparing and revising SOPs.

Minimum Qualifications:

• B.S. / B.A. degree in Biology or related field and a minimum of 5 years of relevant experience in the CRO industry; or, advanced degree in Biology or related field and at least 2 years of relevant experience in the CRO industry.
• Knowledge of GLP regulations and regulatory guidelines.
• Excellent communication skills, both oral and written.
• Strong capabilities for leadership.
• Excellent organizational skills.
• Proficient in the use of basic computer applications such as MS Word and Excel.

Additional Position Requirements:

• Ability to multi-task and produce quality analysis while working under the pressure of strict deadlines.
• Proficient in time management and resource planning.
• Ability to initiate and implement self-development efforts.
• Ability to effectively interact with clients and regulatory personnel.
• Ability to make decisions and complete assignments with minimal supervision.
• Ability to self-direct work priorities.

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